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Dr.Jart Cicapair Tiger Grass Color Correcting Treatment Zinc Oxide, Titanium Dioxide 5.8 g/100mL; 2.8 g/100mL Cream, 5 mL — NDC 49404-0147-01 package photo

Dr.Jart Cicapair Tiger Grass Color Correcting Treatment Zinc Oxide, Titanium Dioxide 5.8 g/100mL; 2.8 g/100mL Cream, 5 mL

by Have & Be Co., Ltd. · 5 mL in 1 JAR (49404-147-01)
NDC 49404-0147-01
🏷️ FDA NDC (as labeled) 49404-147-01 billing pads the product segment with a zero
This package
Contains5 mL Pack sizes5 compare ↓
Also comes in: 1 ml 49404-0147-03 15 mL 49404-0147-05 50 mL 49404-0147-07 10 ml 49404-0147-02
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 49404-147-01
Product NDC 49404-147
11-digit billing NDC 49404014701
UNII SOI2LOH54Z, 15FIX9V2JP
UPC 8809535802002
Application # M020
SPL Set ID 40f96baf-0359-4d68-801f-68562c909446
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-10-28
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 49404-147-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 49404-0147-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerHave & Be Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code49404
First marketedOct 2021
Product typeHuman Otc Drug
Portfolio18 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is a topical cream containing titanium dioxide and zinc oxide, which are mineral ingredients commonly used in over-the-counter sunscreen and skin-barrier products. Both ingredients function as physical blockers that sit on the skin surface. Titanium dioxide and zinc oxide are typically used to help protect skin from ultraviolet rays and to support the skin barrier. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for its category rather than being individually reviewed.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 2FXJ6SW4PK
    A plant extract from yarrow, used in some formulations as a natural flavoring agent or botanical ingredient to add taste or aroma to the medicine.
  • UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII SU125S6473
    Anastatica hierochuntica is a plant material, commonly known as resurrection plant. It serves as a natural emollient and texture agent in formulations, helping to smooth and soften the product's consistency.
  • UNII OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII 7K226YI89Y
    A silicone-based lubricant and anti-foaming agent. It helps reduce friction between tablet particles during manufacturing, prevents foam in liquid formulations, and improves the flow of powders during production.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII 776XM7047L
    Calcium stearate is a white powder derived from stearic acid and calcium. It works as a lubricant and glidant to help the medicine flow smoothly during manufacturing and prevent ingredients from sticking to equipment.
  • UNII UPY805K99W
    A synthetic compound derived from caprylic acid that works as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 6810070TYD
    Centella asiatica leaf is a plant extract used in medicines as a skin-conditioning agent and natural ingredient. It may help soften or soothe the product's texture and is included for its traditional botanical properties in topical or oral formulations.
  • UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII UB27587839
    A plant-derived oil from Roman chamomile flowers. It's used in medicines as a flavoring agent and fragrance to improve taste and smell.
  • UNII X5Z09SU859
    A green pigment made from chromium compounds, used to color tablets and capsules. It helps identify the medicine and makes it visually distinctive without affecting how the drug works.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII RV823G6G67
    Copper gluconate is a salt combining copper and gluconic acid. It serves as a mineral supplement ingredient and color agent in some formulations, providing trace copper content to the medication.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII CG6IX3GCMU
    A natural flavoring extract from wild strawberry fruit. It adds strawberry taste and aroma to make the medicine more pleasant to take, commonly used in chewable tablets and liquid formulations.
  • UNII S72O3284MS
    A plant extract from the gentian root used as a flavoring agent and bitter taste component in some medicines. It helps mask unpleasant tastes and may support digestive formulations.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII YR377U58W9
    Grapefruit oil is a natural aromatic extract from grapefruit peel. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance component.
  • UNII RH041UUZ22
    A plant extract from the houttuynia cordata flower, traditionally used in Asian medicine. In formulations, it may serve as a natural flavoring, coloring, or active botanical ingredient carrier.
  • UNII H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII WEF51750MT
    A synthetic oil derived from branched fatty acids, used as an emollient and lubricant in topical formulations to soften the skin and improve product spreadability and texture.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII 550E4N439V
    A natural plant material derived from cotton seeds, used as a filler or binder in tablets and capsules to add bulk and help hold the medicine's ingredients together in solid form.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII CQD833204Z
    A natural lipid derived from soybean used to help dissolve, stabilize, and improve absorption of active ingredients in medicines. It acts as an emulsifier and solubilizing agent in liquid or injectable formulations.
  • UNII CQ2F5O6YIY
    A natural compound extracted from Centella asiatica plant used as an active skin-conditioning ingredient. It functions as a humectant and skin protectant to improve moisture retention and support skin barrier function in topical formulations.
  • UNII R17X820ROL
    Magnesium aspartate is magnesium combined with the amino acid aspartate. It is used as a mineral supplement ingredient and may help with tablet binding and nutrient delivery in formulations.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII EG97988M5Q
    A synthetic plastic polymer that forms a three-dimensional network. It's used as a coating on tablets and capsules to control how fast the medicine releases into the body, or as a binder to hold pill ingredients together.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII JX7WXJ41DH
    A plant-derived emulsifier made from glycerin and coconut oil. It helps mix oil and water-based ingredients together in the formula and improves how the product spreads or absorbs.
  • UNII 59Z907ZB69
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles, helping powders and tablets flow smoothly during manufacturing and use.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII B46B6DD20U
    Rapeseed sterol is a plant-derived fat obtained from rapeseed oil. It's used in medicines as an emulsifier and thickening agent to help blend oil and water-based ingredients and improve product texture.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII F2522O5L7B
    Rosewood oil is a fragrant plant extract used as a flavoring agent and fragrance component in medicines. It helps mask unpleasant tastes or odors in the medication.
  • UNII EU2PSP0G0W
    Silica dimethyl silylate is a silicon-based powder that acts as a glidant and anti-caking agent. It reduces friction between particles and helps powders flow smoothly during manufacturing and tablet compression.
  • UNII 836SJG51DR
    Sodium ascorbyl phosphate is a derivative of vitamin C that acts as an antioxidant and preservative in medications. It helps protect the drug's active ingredients from degradation caused by air and light exposure.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII 05Q7CD0E49
    A fatty acid derivative made from natural sugar and lauric acid. It acts as an emulsifier and solubilizer in medicines, helping mix water and oil-based ingredients together and improve how the body absorbs certain drugs.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII F84709P2XV
    Wormwood is a plant extract used as a flavoring agent in medicines. It provides a bitter taste to help mask other flavors or make the medication easier to take.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII 80N308T1NN
    Zein is a natural protein extracted from corn. It's used as a film-coating agent and binder in tablets and capsules to improve appearance, protect the medicine, and help it dissolve properly.
  • UNII U6WSN5SQ1Z
    Zinc gluconate is a form of zinc, a mineral, combined with gluconic acid. It's used as a supplement ingredient to provide zinc content in the formulation.

72 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesWATER/AQUA/EAU, ISONONYL ISONONANOATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, ISOTRIDECYL ISONONANOATE, TITANIUM DIOXIDE(CI 77891), METHYLPROPANEDIOL, BIS-HYDROXYETHOXYPROPYL DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, BUTYLOCTYL SALICYLATE, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE, BEESWAX/CERA ALBA/CIRE D'ABEILLE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, GLYCERIN, NIACINAMIDE, DISTEARDIMONIUM HECTORITE, POLYMETHYLSILSESQUIOXANE, MAGNESIUM SULFATE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, CAPRYLYL GLYCOL, CHROMIUM OXIDE GREENS, SYNTHETIC FLUORPHLOGOPITE, IRON OXIDES(CI 77491), GLYCERYL CAPRYLATE, ZEIN, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, ETHYLHEXYLGLYCERIN, CENTELLA ASIATICA LEAF EXTRACT, CITRUS PARADISI (GRAPEFRUIT) PEEL OIL, SILICA DIMETHYL SILYLATE, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL, ALUMINUM HYDROXIDE, ADENOSINE, ZEA MAYS (CORN) STARCH, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HYDROGENATED LECITHIN, CAPRYLHYDROXAMIC ACID, ANTHEMIS NOBILIS FLOWER OIL, TOCOPHEROL, CALCIUM STEARATE, DIPOTASSIUM PHOSPHATE, MADECASSOSIDE, SODIUM CHLORIDE, PANTHENOL, BUTYLENE GLYCOL, ANIBA ROSODORA (ROSEWOOD) WOOD OIL, GOSSYPIUM HERBACEUM (COTTON) EXTRACT, ALCOHOL, ANASTATICA HIEROCHUNTICA EXTRACT, CENTELLA ASIATICA MERISTEM CELL CULTURE, HOUTTUYNIA CORDATA EXTRACT, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, MAGNESIUM ASPARTATE, ZINC GLUCONATE, ARNICA MONTANA FLOWER EXTRACT, LECITHIN, BRASSICA CAMPESTRIS (RAPESEED) STEROLS, ACHILLEA MILLEFOLIUM EXTRACT, GENTIANA LUTEA ROOT EXTRACT, ARTEMISIA ABSINTHIUM EXTRACT, LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, POLYGLYCERYL-2 CAPRATE, SUCROSE LAURATE, CENTELLA ASIATICA EXTRACT, FRAGARIA VESCA (STRAWBERRY) FRUIT EXTRACT, PHENOXYETHANOL, PROPYLENE GLYCOL, GLUCONOLACTONE, COPPER GLUCONATE, CERAMIDE NP, LYSOLECITHIN, CITRIC ACID, XANTHAN GUM, SODIUM ASCORBYL PHOSPHATE, SODIUM BENZOATE, POTASSIUM SORBATE, LIMONENE, LINALOOL

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 1 ml 15 mL 50 mL 10 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dr.Jart Cicapair Tiger Grass Color Correcting Treatment 5.8 g/100mL; 2.8 g/100mLthis 49404-0147-01 Have 5 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2021
On the market since
Oct 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Zinc oxide, titanium dioxide — the ingredient across all brands.

Top reported reactions

Chemical Burn1
Condition Aggravated1
Dehydration1
Erythema1
Erythema Of Eyelid1
Eyelid Irritation1
Eyelid Oedema1

Reporter sex

3 reports
Female · 100%
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
49404-0147-01 You're viewing this 5 mL in 1 JAR (49404-147-01) 2021-10-28 Active
49404-0147-02 10 mL in 1 JAR (49404-147-02) 2021-10-28 Active
49404-0147-03 1 mL in 1 POUCH (49404-147-03) 2021-12-21 Active
49404-0147-05 1 JAR in 1 CARTON (49404-147-05) / 15 mL in 1 JAR (49404-147-04) 2021-12-21 Active
49404-0147-07 1 JAR in 1 CARTON (49404-147-07) / 50 mL in 1 JAR (49404-147-06) 2021-12-21 Active

Pack size FAQ

What quantity is in NDC 49404-0147-01?
NDC 49404-0147-01 contains 5 mL — 5 ml in 1 jar.
What is the difference between NDC 49404-0147-01 and NDC 49404-0147-03?
Both are Dr.Jart Cicapair Tiger Grass Color Correcting Treatment Zinc Oxide, Titanium Dioxide 5.8 g/100mL; 2.8 g/100mL Cream — the drug itself is identical. NDC 49404-0147-01 is the 5 mL package, while NDC 49404-0147-03 is the 1 ml package.
What NDC number is used to bill for this package of Dr.Jart Cicapair Tiger Grass Color Correcting Treatment Zinc Oxide, Titanium Dioxide 5.8 g/100mL; 2.8 g/100mL Cream?
Bill NDC 49404-0147-01 — the 11-digit billing format is 49404014701. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 49404-147-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 49404-0147-01, written without dashes as 49404014701. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 49404-0147-01, the first segment (49404) is the labeler code FDA assigned to Have & Be Co., Ltd.; the middle segment (0147) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Have & Be Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 1 ml (49404-0147-03), 1 jar (49404-0147-05), 1 jar (49404-0147-07). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Have & Be Co., Ltd. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 3 words ▾

Helps prevent sunburn

⏱️ Dosage and Administration 94 words ▾

For Sunscreen use: Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating Sun Protection Measures.

Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: – Limit time in the sun, especially from 10 am - 2 pm Wear long-sleeved shirts, pants, hats and sunglasses Children under 6 months: Ask a doctor

⚠️ Warnings 56 words ▾

For external use only. Do not use on damaged or broken skin. When using this product, keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

📦 Storage and Handling 12 words ▾

Protect the product in this container from excessive heat and direct sunlight

🧪 Active Ingredient 6 words ▾

Zinc Oxide 5.8% Titanium Dioxide 2.8%

🧪 Inactive Ingredients 189 words ▾

WATER/AQUA/EAU, ISONONYL ISONONANOATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, ISOTRIDECYL ISONONANOATE, TITANIUM DIOXIDE(CI 77891), METHYLPROPANEDIOL, BIS-HYDROXYETHOXYPROPYL DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, BUTYLOCTYL SALICYLATE, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE, BEESWAX/CERA ALBA/CIRE D'ABEILLE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, GLYCERIN, NIACINAMIDE, DISTEARDIMONIUM HECTORITE, POLYMETHYLSILSESQUIOXANE, MAGNESIUM SULFATE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, CAPRYLYL GLYCOL, CHROMIUM OXIDE GREENS, SYNTHETIC FLUORPHLOGOPITE, IRON OXIDES(CI 77491), GLYCERYL CAPRYLATE, ZEIN, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, ETHYLHEXYLGLYCERIN, CENTELLA ASIATICA LEAF EXTRACT, CITRUS PARADISI (GRAPEFRUIT) PEEL OIL, SILICA DIMETHYL SILYLATE, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL, ALUMINUM HYDROXIDE, ADENOSINE, ZEA MAYS (CORN) STARCH, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HYDROGENATED LECITHIN, CAPRYLHYDROXAMIC ACID, ANTHEMIS NOBILIS FLOWER OIL, TOCOPHEROL, CALCIUM STEARATE, DIPOTASSIUM PHOSPHATE, MADECASSOSIDE, SODIUM CHLORIDE, PANTHENOL, BUTYLENE GLYCOL, ANIBA ROSODORA (ROSEWOOD) WOOD OIL, GOSSYPIUM HERBACEUM (COTTON) EXTRACT, ALCOHOL, ANASTATICA HIEROCHUNTICA EXTRACT, CENTELLA ASIATICA MERISTEM CELL CULTURE, HOUTTUYNIA CORDATA EXTRACT, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, MAGNESIUM ASPARTATE, ZINC GLUCONATE, ARNICA MONTANA FLOWER EXTRACT, LECITHIN, BRASSICA CAMPESTRIS (RAPESEED) STEROLS, ACHILLEA MILLEFOLIUM EXTRACT, GENTIANA LUTEA ROOT EXTRACT, ARTEMISIA ABSINTHIUM EXTRACT, LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, POLYGLYCERYL-2 CAPRATE, SUCROSE LAURATE, CENTELLA ASIATICA EXTRACT, FRAGARIA VESCA (STRAWBERRY) FRUIT EXTRACT, PHENOXYETHANOL, PROPYLENE GLYCOL, GLUCONOLACTONE, COPPER GLUCONATE, CERAMIDE NP, LYSOLECITHIN, CITRIC ACID, XANTHAN GUM, SODIUM ASCORBYL PHOSPHATE, SODIUM BENZOATE, POTASSIUM SORBATE, LIMONENE, LINALOOL

🎯 Purpose 1 words ▾

Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 49401-0102-01 · GlaxoSmithKline 49404-0148-02 · Have →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.