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Ultra Violette Future Screen Broad Spectrum SPF 50 ZINC OXIDE 200 mg/mL Lotion, 15 mL — NDC 84803-0103-15 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ultra Violette Future Screen Broad Spectrum SPF 50 ZINC OXIDE 200 mg/mL Lotion, 15 mL — NDC 84803-103-15 (Billing 84803-0103-15)

by Grace and Fire USA Inc. · 15 mL in 1 BOTTLE

This is a package of 15 mL of Ultra Violette Future Screen Broad Spectrum SPF 50 ZINC OXIDE 200 mg/mL Lotion from Grace and Fire USA Inc., marketed since Dec 2024 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 84803-0103-15
🏷️ FDA NDC (as labeled) 84803-103-15 billing pads the product segment with a zero
This package
Contains15 mL Pack sizes3 compare ↓
Main listing for product 84803-103 · Also comes in: 20 ml 84803-103-20 50 ml 84803-103-50
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84803-103-15
Product NDC 84803-103
11-digit billing NDC 84803010315
UNII SOI2LOH54Z
Application # M020
SPL Set ID 252fdc91-bbe2-58ec-e063-6294a90a5067
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-12-01
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 84803-103-15 — 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 → 84803-0103-15. 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.

Clinical

🧪 What is this product?

This is a topical lotion containing zinc oxide, marketed as an over-the-counter sunscreen product under FDA's monograph rules for sunscreen drugs. Zinc oxide is a mineral UV filter that is typically used in sunscreens to help block ultraviolet radiation from the sun. The product is formulated to provide broad-spectrum protection and is labeled with SPF 50.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
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.

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: 20 ml 50 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
84803-0103-15 You're viewing this Main listing 15 mL in 1 BOTTLE 2024-12-01 — Active
84803-0103-20 84803-103-20 20 mL in 1 BOTTLE, PLASTIC 2024-12-01 — Active
84803-0103-50 84803-103-50 50 mL in 1 BOTTLE 2024-12-01 — Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 15 mL — 15 ml in 1 bottle.
How does this package differ from NDC 84803-0103-20?
Both are Ultra Violette Future Screen Broad Spectrum SPF 50 ZINC OXIDE 200 mg/mL Lotion — the drug itself is identical. This page's package is the 15 mL one, while NDC 84803-0103-20 is the 20 ml package.
What NDC number is used to bill for this package of Ultra Violette Future Screen Broad Spectrum SPF 50 ZINC OXIDE 200 mg/mL Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lilikoi Mineral Defense Sport Sunscreen SPF 30 200 mg/mL 15751-3040-05 Eminence 1 tube — — FDA listed —
Eminence Tropical Vanilla Day Cream SPF 40 Sunscreen 200 mg/mL 15751-3500-01 Eminence 1 jar — — Discontinued —
Eminence Lilikoi Daily Defense Moisturizer SPF 40 Sunscreen 200 mg/mL 15751-3501-01 Eminence 1 jar — — FDA listed —
Eminence Bright Skin Moisturizer SPF 40 Sunscreen 200 mg/mL 15751-3503-01 Eminence 1 jar — — FDA listed —
Sport Broad Spectrum SPF50 Water Resistant 80 minutes Mineral Sunscreen UVA UVB Protection Stick 200 mg/mL 53675-0203-00 Aruba 30 ml — — FDA listed —
Broad Spectrum SPF50 Water Resistant (80 minutes) Mineral Sunscreen UVA UVB Protection Stick for Kids 200 mg/mL 53675-0205-00 Aruba 30 ml — — FDA listed —
THINKSPORT sunscreen SPF 50 200 mg/mL 60781-1001-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKSPORT Kids sunscreen SPF 50 200 mg/mL 60781-1002-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKBABY Baby Sunscreen SPF 50 200 mg/mL 60781-1003-03 thinkOperations,LLC 89 ml — — FDA listed —
Think Every Day Face Sunscreen SPF 30 200 mg/mL 60781-1011-01 thinkOperations,LLC 59 ml — — FDA listed —
Think Aloe and Tea Leaves Zinc oxide 200 mg/mL 60781-4698-01 thinkOperations,LLC 89 ml — — FDA listed —
Raw Elements Daily Moisturizer Broad Spectrum SPF30 200 mg/mL 70680-0305-00 Raw 80 ml — — FDA listed —
SUNNY Q Broad Spectrum SPF-30 200 mg/mL 81738-0138-00 Sunny 100.55 ml — — FDA listed —
TIGER BABY Baby Sunscreen SPF-50 200 mg/mL 82247-0278-00 BRICKELL 5 ml — — FDA listed —
JOYSPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0354-00 JOYSPRING 30 ml — — FDA listed —
JOY SPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0356-00 JOYSPRING 90 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 2w 200 mg/mL 76354-0471-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Super Shield Mineral Sunscreen SPF50 200 mg/mL 79265-7778-01 Babo 89 ml — — FDA listed —
GLC OG Natural Tinted SPF 30 Sunscreen 200 mg/mL 84747-0530-00 GUD 1 jar — — FDA listed —
Sun Bum 50 Mineral Sunscreen 1 OZ 200 mg/mL 69039-0797-01 Sun 30 ml — — FDA listed —
Everyday Coverage Tinted Sunscreen - Extra Light Tint 200 mg/mL 72592-0001-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 9w 200 mg/mL 76354-0474-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 14w 200 mg/mL 76354-0479-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 3N 200 mg/mL 76354-0480-01 e.l.f. 1 bottle — — FDA listed —
Dr. Mercola Broad Spectrum 200 mg/mL 71239-0787-23 Natural 236 ml — — FDA listed —
Vitamin C BB Beauty Balm Sheer Tint SFP 30 200 mg/mL 55560-0108-01 Andalou 1 tube — — FDA listed —
Everyday Coverage Tinted Sunscreen - Light Tint 200 mg/mL 72592-0002-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 12w 200 mg/mL 76354-0477-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 5N 200 mg/mL 76354-0481-01 e.l.f. 1 bottle — — FDA listed —
Derma E Vitamin C Weightless Moisturizer SPF 45 200 mg/mL 54108-0359-01 derma 1 bottle — — FDA listed —
Kypris Pot of Shade Heliotropic Broad Spectrum SPF 30 Sunscreen And Primer 200 mg/mL 70608-0001-01 Kypris 1 jar — — FDA listed —
Everyday Coverage Tinted Sunscreen - Medium Tint 200 mg/mL 72592-0003-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 13w 200 mg/mL 76354-0478-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color plus Correct Sheer Beige SPF 30 200 mg/mL 55560-0110-01 Andalou 1 tube — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 1C 200 mg/mL 76354-0470-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 11w 200 mg/mL 76354-0476-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 8N 200 mg/mL 76354-0483-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50 200 mg/mL 79265-8758-01 Babo 89 ml — — FDA listed —
Thinkbaby Clear Zinc SPF 30 200 mg/mL 60781-4175-03 thinkOperations,LLC 89 ml — — FDA listed —
Baby Bum Mineral 50 Sunscreen 200 mg/mL 69039-0686-00 Sun 88 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 4W 200 mg/mL 76354-0472-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 7N 200 mg/mL 76354-0482-01 e.l.f. 1 bottle — — FDA listed —
Perfecting BB Beauty Balm Natural Tint SPF 30 200 mg/mL 55560-0104-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 200 mg/mL 69039-0728-01 Sun 88 ml — — FDA listed —
Vivaiodays Sunscreen with Turmeric 200 mg/mL 71778-0002-01 5SENCO 100 ml — — FDA listed —
Ultra Violette Future Screen Broad Spectrum SPF 50 200 mg/mLthis 84803-0103-15 Grace 15 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 10w 200 mg/mL 76354-0475-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color Plus Correct Sheer Tan SPF 30 200 mg/mL 55560-0106-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 32 OZ 200 mg/mL 69039-0718-01 Sun 946 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 6w 200 mg/mL 76354-0473-01 e.l.f. 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

🏛️
2024
On the market since
Dec 2024
📍
2026
Currently FDA-listed
2 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.

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 I9PJ0O6294
    A modified starch derived from corn or potato starch with aluminum salt and octenylsuccinic acid added. It acts as a binder to hold tablet ingredients together and as a thickening agent in liquid formulations.
  • UNII F01RIY4371
    A synthetic polymer made from acrylic compounds and taurate, this substance acts as a thickener and stabilizer. It helps give liquid medicines a smooth texture and keeps ingredients from separating.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • 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 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 XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • 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 8D9H4QU99H
    A synthetic fatty acid ester derived from coconut oil, used as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the body absorbs certain drugs.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII P7E6YFV72X
    Diisopropyl adipate is a clear, oily liquid derived from adipic acid. It acts as a plasticizer and solvent in medicines, helping soften coatings and improve how the drug dissolves or spreads in the body.
  • 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 NLE5KIG74K
    A plant-based oily substance made from glycerin and citric acid. It helps keep oil and water mixed together in the medicine and may aid in dissolving or delivering active ingredients.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII 6M3P64V0NC
    A fine powder made from magnesium, aluminum, and silicon compounds. It absorbs moisture and helps keep medicine ingredients from clumping or separating, so the product stays stable and flows smoothly during manufacturing.
  • 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 820DPX33S7
    A synthetic emulsifier derived from glycerin and fatty acids. It helps mix oil and water-based ingredients together and keeps them evenly blended throughout the product.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • 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 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII W8K377W98I
    A mixture of sugars made by rearranging glucose molecules. It acts as a sweetener and filler to improve taste and add bulk to the medicine while helping it hold together.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII GW89575KF9
    Squalane is a lightweight oil derived from plant sources or synthesized. It acts as an emollient and lubricant in formulations, helping ingredients blend smoothly and improving product texture and spreadability.
  • 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.

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

The official label also statesWater, Diisopropyl Adipate, Coco-Caprylate/Caprate, Ethylhexyl Methoxycrylene, C12-15 Alkyl Benzoate, Glyceryl Oleate Citrate, Propanediol, Decyl Glucoside, Polyglyceryl-4 Isostearate, Squalane, Aluminum Starch Octenylsuccinate, Saccharide Isomerate, Tocopheryl Acetate, Caprylic/Capric Triglyceride, Triethoxycaprylylsilane, Magnesium Aluminum Silicate, Citric Acid, Sodium Citrate, Hydroxyacetophenone, Potassium Cetyl Phosphate, Phenoxyethanol, Polyhydroxystearic Acid, Ammonium Polyacryloyldimethyl Taurate, Lactic Acid, Sodium Hydroxide, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499)

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.

Manufacturer & labeler

LabelerGrace and Fire USA Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84803
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio13 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.

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 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 95 words ▾

Directions apply liberally and evenly 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 a.m. – 2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses children under 6 months of age: Ask a doctor

⚠️ Warnings 50 words ▾

FOR EXTERNAL USE ONLY 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 CHILDREN If swallowed, get medical help or contact a Poison Control Center right away

📦 Storage and Handling 11 words ▾

Other Information Protect this product from excessive heat and direct sun

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENTS ZINC OXIDE 20%

🧪 Inactive Ingredients 63 words ▾

Inactive Ingredients Water, Diisopropyl Adipate, Coco-Caprylate/Caprate, Ethylhexyl Methoxycrylene, C12-15 Alkyl Benzoate, Glyceryl Oleate Citrate, Propanediol, Decyl Glucoside, Polyglyceryl-4 Isostearate, Squalane, Aluminum Starch Octenylsuccinate, Saccharide Isomerate, Tocopheryl Acetate, Caprylic/Capric Triglyceride, Triethoxycaprylylsilane, Magnesium Aluminum Silicate, Citric Acid, Sodium Citrate, Hydroxyacetophenone, Potassium Cetyl Phosphate, Phenoxyethanol, Polyhydroxystearic Acid, Ammonium Polyacryloyldimethyl Taurate, Lactic Acid, Sodium Hydroxide, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499)

🎯 Purpose 2 words ▾

PURPOSE SUNSCREEN

📄 Do Not Use 9 words ▾

FOR EXTERNAL USE ONLY

on damaged or broken skin

📄 When Using This Product 13 words ▾

WHEN USING THIS PRODUCT keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 9 words ▾

STOP USE AND ASK A DOCTOR IF rash occurs

📄 Keep Out of Reach of Children 19 words ▾

KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away

📄 Package Label / Principal Display Panel 20 words ▾

Principal Display Panel Ultra Violette Future Screen Broad Spectrum SPF 50

1.7FL. OZ. (50 mL) UV FUTURE SCREEN US

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Grace and Fire USA 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 2 other package presentations of this same product, including 20 ml (84803-0103-20), 50 ml (84803-0103-50). 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?
Grace and Fire USA 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.
← 84803-0102-00 · Grace 84803-0104-01 · Grace →
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.