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Eucerin Sensitive Mineral SPF 50 Sunscreen Zinc Oxide 24 g/100g Lotion, 14 g — NDC 66800-1000-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Eucerin Sensitive Mineral SPF 50 Sunscreen Zinc Oxide 24 g/100g Lotion, 14 g — NDC 66800-1000-2 (Billing 66800-1000-02)

by Beiersdorf Inc · 14 g in 1 POUCH

This is a package of 14 g of Eucerin Sensitive Mineral SPF 50 Sunscreen Zinc Oxide 24 g/100g Lotion from Beiersdorf Inc, marketed since Nov 2021 and currently FDA-listed.

NDC 66800-1000-02
🏷️ FDA NDC (as labeled) 66800-1000-2 billing pads the package segment with a zero
This package
Contains14 g Pack sizes2 compare ↓
Product page 66800-1000-01 Also comes in: 118 g 66800-1000-1
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

NDC database record

One package, one record: these facts belong to NDC 66800-1000-2 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66800 labeler · 1000 product · 2 package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0072140032265
FDA record last changed
Jul 24, 2026
⚠️
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) 66800-1000-2
Product NDC 66800-1000
11-digit billing NDC 66800100002
UNII SOI2LOH54Z
UPC 0072140032265
Application # M020
SPL Set ID cdb25154-e4e3-efc7-e053-2a95a90a2df6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-11-03
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 66800-1000-2 — a 5-4-1 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 package segment → 66800-1000-02. 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 an over-the-counter mineral sunscreen lotion applied to skin. It contains zinc oxide, a physical (mineral) UV filter that works by sitting on the skin surface to reflect and scatter ultraviolet rays. Sunscreens with zinc oxide are typically used to help protect skin from sun damage during outdoor activity. This product is marketed under the FDA's over-the-counter monograph rules for sunscreen ingredients.

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: 118 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
66800-1000-01 66800-1000-1 Main listing 118 g in 1 TUBE 2021-11-03 — Active
66800-1000-02 You're viewing this 14 g in 1 POUCH 2023-03-03 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 14 g — 14 g in 1 pouch.
How does this package differ from NDC 66800-1000-01?
Both are Eucerin Sensitive Mineral SPF 50 Sunscreen Zinc Oxide 24 g/100g Lotion — the drug itself is identical. This page's package is the 14 g one, while NDC 66800-1000-01 is the 118 g package.
What NDC number is used to bill for this package of Eucerin Sensitive Mineral SPF 50 Sunscreen Zinc Oxide 24 g/100g 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
Clearly Zinq Mineral Gel Sunscreen BS SPF 60 24 g/100g 62742-4236-01 Allure 96 g — — FDA listed —
ATTITUDE Sunly Kids Mineral sunscreen SPF 50 Watermelon and coco 24 g/100g 61649-0527-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sunly Mineral Sunscreen Face Stick SPF 50 Unscented 24 g/100g 61649-0560-02 9055-7588 1 tube — — FDA listed —
ATTITUDE Sunly Kids Mineral Sunscreen Face Stick SPF 50 Unscented 24 g/100g 61649-0562-02 9055-7588 1 tube — — FDA listed —
Eucerin Baby Sensitive Mineral SPF 50 Sunscreen 24 g/100g 66800-4000-01 Beiersdorf 118 g — — FDA listed —
Lino 24 g/100g 84749-0001-01 Lino 30 g — — FDA listed —
ATTITUDE Sunly Kids Mineral Sunscreen Stick SPF 50 Watermelon and Coco 24 g/100g 61649-0547-01 9055-7588 60 g — — FDA listed —
ATTITUDE Sunly Baby Mineral Sunscreen Face Stick SPF 50 Unscented 24 g/100g 61649-0561-02 9055-7588 1 tube — — FDA listed —
ATTITUDE Sunly Baby Mineral sunscreen SPF 50 Unscented 24 g/100g 61649-0521-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sunly Mineral Sunscreen Stick SPF 50 Unscented 24 g/100g 61649-0540-01 9055-7588 60 g — — FDA listed —
Land Shark Zinky SPF 36 Pacific Purple 24 g/100g 52854-0645-01 Tropical 14 g — — FDA listed —
ATTITUDE Oceanly Phyto-Sun Tinted Cream SPF 30 24 g/100g 61649-0070-30 9055-7588 30 g — — FDA listed —
ATTITUDE Oceanly Phyto-Sun Tinted Oil SPF 30 24 g/100g 61649-0073-08 9055-7588 8.5 g — — FDA listed —
ATTITUDE Sunly Kids Mineral Sunscreen Stick SPF 50 Unscented 24 g/100g 61649-0542-01 9055-7588 60 g — — FDA listed —
ATTITUDE Sensitive natural Mineral Sunscreen Stick SPF 50 Unscented 24 g/100g 61649-0544-01 9055-7588 60 g — — FDA listed —
Land Shark Zinky SPF 36 Azure Blue 24 g/100g 52854-0615-01 Tropical 14 g — — FDA listed —
ATTITUDE Oceanly Phyto-Sun Tinted Shimmer Cream SPF 30 24 g/100g 61649-0071-08 9055-7588 8.5 g — — FDA listed —
ATTITUDE Sunly Kids Mineral sunscreen SPF 50 Unscented 24 g/100g 61649-0522-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sensitive natural baby Mineral sunscreen SPF 50 Unscented 24 g/100g 61649-0524-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sunly Mineral Sunscreen Stick SPF 50 Sun kissed vanilla 24 g/100g 61649-0548-01 9055-7588 60 g — — FDA listed —
ATTITUDE Sunly Mineral sunscreen SPF 50 Tropical coco 24 g/100g 61649-0523-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sunly Mineral sunscreen SPF 50 Sun kissed vanilla 24 g/100g 61649-0528-01 9055-7588 85 g — — FDA listed —
Land Shark Zinky SPF 36 Pink Beach 24 g/100g 52854-0625-01 Tropical 14 g — — FDA listed —
ATTITUDE Sunly Mineral sunscreen SPF 50 Unscented 24 g/100g 61649-0520-01 9055-7588 85 g — — FDA listed —
ATTITUDE Sunly Baby Mineral Sunscreen Stick SPF 50 Unscented 24 g/100g 61649-0541-01 9055-7588 60 g — — FDA listed —
ATTITUDE Sunly Mineral Sunscreen Stick SPF 50 Tropical coco 24 g/100g 61649-0543-01 9055-7588 60 g — — FDA listed —
Eucerin Sensitive Mineral SPF 50 Sunscreen 24 g/100gthis 66800-1000-02 Beiersdorf 14 g — — FDA listed —
Utu Broad Spectrum SPF 50 Tinted Sunscreen-Stick 24 g/100g 87952-0001-02 Utu 28 g — — 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
Nov 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.

What it looks like

Color white
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 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 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 TY3J98ZR7R
    A synthetic polymer that acts as a film-former and texture enhancer in topical formulations. It helps create a smooth, long-wearing coating on skin and improves how the product spreads and adheres.
  • 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 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 V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 3V5U97P248
    A synthetic organic compound used as a UV filter and stabilizer in medications. It helps protect the drug from light degradation and may improve shelf life in formulations exposed to sunlight.
  • 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 3YU1SQ04DV
    A synthetic oily liquid derived from pelargonic acid and ethylhexanol. It functions as an emollient and penetration enhancer in topical formulations, helping the medicine spread smoothly on skin and improving ingredient absorption.
  • UNII P540XA09DR
    Enoxolone is a naturally derived compound from licorice root that acts as a skin-soothing and anti-inflammatory agent. In medicines, it helps reduce irritation and supports the healing of mucous membranes or damaged skin.
  • UNII 1MV1Z7MKVQ
    A plant extract from licorice root used as a natural sweetener and flavoring agent in medicines. It may also help soothe throat irritation and improve taste.
  • 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 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 0841698D2F
    A synthetic polymer used as a film-coating agent to protect tablets and capsules. It helps control how quickly the medicine dissolves and improves the appearance of the finished product.
  • 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 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 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 08MNR5YE2R
    A wax made in a laboratory to mimic natural beeswax. It's used as a coating, binder, and thickener to give medicines a smooth texture and protect them from moisture.
  • 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.

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

The official label also statesWater, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Butyloctyl Salicylate, Ethylhexyl Pelargonate, Cetyl PEG/PPG-10/1 Dimethicone, Propylene Glycol, Cyclopentasiloxane, Bis-Octyldodecyl Dimer Dilinoleate/Propanediol Copolymer, Dimethicone, Diethylhexyl Syringylidenemalonate, Ethylhexyl Methoxycrylene, Polyester-27, Glycyrrhetinic Acid, Glycyrrhiza Inflata Root Extract, Tocopherol (Vitamin E), Sodium Ascorbyl Phosphate, Beeswax, Hydroxyacetophenone, Caprylyl Glycol, 1,2-Hexanediol, PEG-12 Dimethicone Crosspolymer, Triethoxycaprylylsilane, Sodium Chloride

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

LabelerBeiersdorf Inc
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code66800
First marketedNov 2021
Product typeHuman Otc Drug
Portfolio106 products on file

More NDCs from Beiersdorf Inc labeler code 66800

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 🧪 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses ■ 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 102 words ▾

Directions ■ apply liberally 15 minutes before sun exposure ■ reapply: ■ after 80 minutes of swimming or sweating ■ immediately after towel drying ■ at least every 2 hours ■ 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-sleeve shirts, pants, hats, and sunglasses ■ children under 6 months: Ask a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 4 words ▾

Active ingredient Zinc Oxide

🧪 Inactive Ingredients 51 words ▾

Inactive ingredients Water, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Butyloctyl Salicylate, Ethylhexyl Pelargonate, Cetyl PEG/PPG-10/1 Dimethicone, Propylene Glycol, Cyclopentasiloxane, Bis-Octyldodecyl Dimer Dilinoleate/Propanediol Copolymer, Dimethicone, Diethylhexyl Syringylidenemalonate, Ethylhexyl Methoxycrylene, Polyester-27, Glycyrrhetinic Acid, Glycyrrhiza Inflata Root Extract, Tocopherol (Vitamin E), Sodium Ascorbyl Phosphate, Beeswax, Hydroxyacetophenone, Caprylyl Glycol, 1,2-Hexanediol, PEG-12 Dimethicone Crosspolymer, Triethoxycaprylylsilane, Sodium Chloride

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 8 words ▾

Do not use 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 occures

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 2 words ▾

Questions? 1-800-227-4703

📄 Package Label / Principal Display Panel 41 words ▾

Eucerin ® Sensitive Mineral Zinc Oxide Protection Lightweight Sunscreen Lotion 50 Broad Spectrum SPF 50 Hypoallergenic | Fragrance Free No Oxybenzone and Octinoxate 5 AOX Shield Antioxidant Defense Developed With Dermatologists Water Resistant (80 Minutes) 4 FL OZ (118 mL) eucsensmineralBA07

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

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 Eucerin Sensitive Mineral SPF 50 Sunscreen (this brand).

Top reported reactions

Macular Degeneration460
Pyrexia306
Nausea290
Pain282
Malaise261
Weight Decreased236
Therapeutic Product Effect Incomplete214

Age at onset

Neonate5
Infant8
Child28
Adolescent5
Adult110
Elderly192

Reporter sex

1,941 reports
Male · 37%
Female · 63%
Unknown · 0%

Serious outcomes

Hospitalization988
Death204
Life-threatening116
Disabling32
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 272 0
Most recent year is provisional (FAERS lags ~3 months).
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.

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 Beiersdorf 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 1 other package presentation of this same product, including 118 g (66800-1000-01). 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?
Beiersdorf 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.
← 66800-0381-03 · Beiersdorf 66800-1093-07 · Beiersdorf →
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.