Home › NDC Lookup › Ingredients › White Tea Tinted Moisturizer Broad Spect... › 83022-0077-15
WHITE TEA TINTED MOISTURIZER 10 mg/g; 3 mg/g; 5 mg/g; 7 mg/g Cream — NDC 83022-0077-15 package photo

WHITE TEA TINTED MOISTURIZER 10 mg/g; 3 mg/g; 5 mg/g; 7 mg/g Cream

by GLOW CONCEPT INC · 1 BOTTLE, PUMP in 1 CARTON (83022-077-15) / 30 g in 1 BOTTLE, PUMP
NDC 83022-0077-15
🏷️ FDA NDC (as labeled) 83022-077-15 billing pads the product segment with a zero
This package
Contains30 g in 1 bottle, pump Pack sizes7 compare ↓
Also comes in: 30 g 83022-0077-17 30 g 83022-0077-11 30 g 83022-0077-12 30 g 83022-0077-13 30 g 83022-0077-14 30 g 83022-0077-16
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) 83022-077-15
Product NDC 83022-077
11-digit billing NDC 83022007715
UNII V06SV4M95S, G63QQF2NOX, 4X49Y0596W, 5A68WGF6WM
UPC 0818324023250, 0818324023496, 0818324021683, 0818324023533 +2 more
Application # M020
SPL Set ID eb2df93f-6cdc-7ae8-e053-2a95a90a0091
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-10-21
Route TOPICAL
Dosage form CREAM
Substance HOMOSALATE; AVOBENZONE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 83022-077-15 — 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 → 83022-0077-15. 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

LabelerGLOW CONCEPT INC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code83022
First marketedOct 2022
Product typeHuman Otc Drug
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 moisturizer that contains four sunscreen active ingredients: avobenzone, homosalate, octisalate, and octocrylene. These ingredients function as ultraviolet (UV) filters, typically used to help protect skin from sun exposure when applied to exposed areas. The product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for sunscreen products rather than being individually reviewed as a new drug application.

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.

💊 What it looks like

Color brown
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 1N032N7MFO
    A brown-colored mineral form of iron oxide used as a colorant in tablets and capsules. It gives medicines their brown or tan appearance without affecting how the drug works.
  • UNII 9I2BJY2J17
    A plant extract from tea flowers used as a natural coloring agent and antioxidant in medicines. It helps maintain product stability and may provide a subtle color to the formulation.
  • 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 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII S3KFG6Q5X8
    An organic chemical compound used as a UV filter in topical formulations. It helps protect the medicine or product from degradation caused by sunlight exposure during storage and use.
  • 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 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • 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 KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII Y6O7T4G8P9
    Hydrated silica is a fine powder form of silicon dioxide with absorbed water. It works as an anti-caking agent and absorbent in medicines, helping powders stay free-flowing and preventing clumping.
  • UNII 86FQE96TZ4
    A synthetic polymer, this ingredient acts as a thickener and suspending agent in liquid formulations. It helps maintain uniform consistency and keeps particles evenly distributed throughout the medicine.
  • UNII AR294KAG3T
    Isoeicosane is a synthetic hydrocarbon liquid used as a solvent and vehicle in medicines. It helps dissolve or suspend active ingredients and improves product stability and texture.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • 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 CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • UNII D9B634V4GP
    A plant extract from pomegranate flowers used as a natural colorant, flavoring agent, or antioxidant in medicines. It helps preserve product stability and may contribute to the medicine's taste or appearance.
  • UNII 0W8RRI5W5A
    A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

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

The official label also statesWater (Aqua), Titanium Dioxide (CI 77891), Potassium Cetyl Phosphate, Glycerin, Ethylhexyl Methoxycrylene, Cetearyl Alcohol, Cetyl Dimethicone, Dimethicone, Isoeicosane, Silica, Sorbitan Sesquioleate, Hydroxyethylacrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 60, Phenoxyethanol, Fragrance, Caprylyl Glycol, Iron Oxide (CI 77492), Hexylene Glycol, Ethylhexylglycerin, Iron Oxide (CI 77491), Tocopheryl Acetate, Iron Oxide (CI 77499), Tetrahexyldecyl Ascorbate, Camellia Sinensis (White Tea) Leaf Extract, Punica Granatum (Pomegranate) Extract.

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: 30 g 30 g 30 g 30 g 30 g 30 g
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
White Tea Tinted Moisturizer 10 mg/g; 3 mg/g; 5 mg/g; 7 mg/gthis 83022-0077-15 GLOW 1 bottle — — 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

🏛️
2022
On the market since
Oct 2022
📍
2026
Currently FDA-listed
4 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
83022-0077-17 1 BOTTLE, PUMP in 1 CARTON (83022-077-17) / 30 g in 1 BOTTLE, PUMP (83022-077-07) 2022-10-21 Active
83022-0077-11 1 BOTTLE, PUMP in 1 CARTON (83022-077-11) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active
83022-0077-12 1 BOTTLE, PUMP in 1 CARTON (83022-077-12) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active
83022-0077-13 1 BOTTLE, PUMP in 1 CARTON (83022-077-13) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active
83022-0077-14 1 BOTTLE, PUMP in 1 CARTON (83022-077-14) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active
83022-0077-15 You're viewing this 1 BOTTLE, PUMP in 1 CARTON (83022-077-15) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active
83022-0077-16 1 BOTTLE, PUMP in 1 CARTON (83022-077-16) / 30 g in 1 BOTTLE, PUMP 2022-10-21 Active

Pack size FAQ

What quantity is in NDC 83022-0077-15?
NDC 83022-0077-15 is listed by the FDA — 1 bottle, pump in 1 carton / 30 g in 1 bottle, pump.
What NDC number is used to bill for this package of WHITE TEA TINTED MOISTURIZER 10 mg/g; 3 mg/g; 5 mg/g; 7 mg/g Cream?
Bill NDC 83022-0077-15 — the 11-digit billing format is 83022007715. 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 83022-077-15, 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: 83022-0077-15, written without dashes as 83022007715. 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 83022-0077-15, the first segment (83022) is the labeler code FDA assigned to GLOW CONCEPT INC; the middle segment (0077) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (15) 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 GLOW CONCEPT INC. 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 6 other package presentations of this same product, including 1 bottle (83022-0077-17), 1 bottle (83022-0077-11), 1 bottle (83022-0077-12). 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?
GLOW CONCEPT INC 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 👥 Use in Specific Populations 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 29 words ▾

USE Helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 88 words ▾

DIRECTIONS Apply liberally 15 minutes before sun exposure • Use a water resistant sunscreen if swimming or sweating • reapply at least every two hours • Sun Protection Measures • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • Limit time in sun, especially from 10 a.m. – 2 p.m. • Wear long-sleeve shirts, pants, hats, and sunglasses

⚠️ Warnings 58 words ▾

WARNINGS 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 doctor if • rash occurs. Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away.

👥 Use in Specific Populations 7 words ▾

CHILDREN UNDER 6 MONTHS Ask a doctor.

🧪 Active Ingredient 10 words ▾

ACTIVE INGREDIENT Avobenzone...... 3% Homosalate....... 10% Octisalate........... 5% Octocrylene........ 7%

🧪 Inactive Ingredients 64 words ▾

INACTIVE INGREDIENT SECTION Water (Aqua), Titanium Dioxide (CI 77891), Potassium Cetyl Phosphate, Glycerin, Ethylhexyl Methoxycrylene, Cetearyl Alcohol, Cetyl Dimethicone, Dimethicone, Isoeicosane, Silica, Sorbitan Sesquioleate, Hydroxyethylacrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 60, Phenoxyethanol, Fragrance, Caprylyl Glycol, Iron Oxide (CI 77492), Hexylene Glycol, Ethylhexylglycerin, Iron Oxide (CI 77491), Tocopheryl Acetate, Iron Oxide (CI 77499), Tetrahexyldecyl Ascorbate, Camellia Sinensis (White Tea) Leaf Extract, Punica Granatum (Pomegranate) Extract.

🎯 Purpose 2 words ▾

PURPOSE SUNSCREEN

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83021-0877-07 · ANUBIS 83027-0001-01 · Nutritional →
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.