Zinc Oxide 20 g/100g Ointment, 1 tube
by Geri-Gentle Corporation · 1 TUBE in 1 BOX (69771-109-39) / 56.8 g in 1 TUBE
NDC 69771-0109-39
🏷️ FDA NDC (as labeled)
69771-109-39
billing pads the product segment with a zero
This package
Contains1 tube
Pack sizes2 compare ↓
Also comes in:
28.4 g 69771-0109-38
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
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
FDA NDC (as labeled)
69771-109-39
Product NDC
69771-109
11-digit billing NDC
69771010939
RxCUI
198911
UNII
SOI2LOH54Z
UPC
0648289167108
Application #
M016
SPL Set ID
f5cfab62-8aab-4109-b15b-4fe380f7cb9e
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2017-01-15
Route
TOPICAL
Dosage form
OINTMENT
Substance
ZINC OXIDE
Why two NDCs?
The FDA registers this code as 69771-109-39 — 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 → 69771-0109-39. 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
LabelerGeri-Gentle Corporation
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code69771
First marketedJan 2017
Product typeHuman Otc Drug
Portfolio22 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 ointment containing 20% zinc oxide, marketed as an over-the-counter monograph product. Zinc oxide is commonly used in skin-care preparations to help protect and soothe the skin. It is typically found in products such as diaper rash treatments, barrier creams, and skin protectants meant to shield skin from moisture and irritation.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:
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.
💬 Questions about Zinc Oxide?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 I835H2IHHX
A waxy substance derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water ingredients together and keep them blended throughout the product's shelf life.
-
UNII 2DMT128M1S
A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
-
UNII 7EV65EAW6H
Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
-
UNII N6K5787QVP
Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.
-
UNII 4T6H12BN9U
Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesCetostearyl Alcohol, Cetomacrogol 1000, Lanolin, Light Liquid Paraffin, White Soft Paraffin
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 system | Per g | Per 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:
28.4 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Zinc Oxide 20 g/100g 68001-0533-50 | BluePoint | 454 g | $0.016 | — | Availability likely | — |
| Leader Zinc Oxide 200 mg/g 70000-0334-01 | Cardinal | 454 g | $0.016 | — | Availability likely | — |
| Good Neighbor Pharmacy Skin Protectant .2 g/g 46122-0676-46 | AMERISOURCE | 1 tube | $0.036 | — | Availability likely | — |
| Rugby Zinc Oxide 20% 20 g/100g 00536-1316-25 | Rugby | 72 tubes | $0.059 | — | Availability likely | — |
| Zinc Oxide 20 g/100g 68001-0532-45 | BluePoint | 1 tube | $0.079 | — | Availability likely | — |
| Nivagen Zinc Oxide 200 mg/g 75834-0170-01 | Nivagen | 28.4 g | $0.107 | — | Availability likely | — |
| Sheffield Zinc Oxide 200 mg/g 11527-0065-34 | Sheffield | 1 tube | — | — | FDA listed | — |
| CAREALL Zinc Oxide .2 g/g 51824-0032-03 | New | 28 g | — | — | FDA listed | — |
| ProCure Zinc Oxide 20 g/100g 55681-0017-01 | Twin | 28.3 g | — | — | FDA listed | — |
| Procure 20 g/100g 55681-0304-03 | TWIN | 28.3 g | — | — | FDA listed | — |
| Endit Zinc Oxide Skin Protectant 20 g/100g 64068-0402-01 | Endit | 454 g | — | — | FDA listed | — |
| Endit zinc oxide skin protection 200 mg/g 64068-0500-01 | EndIt | 56.7 g | — | — | FDA listed | — |
| Zinc Oxide .2 g/g 64772-0201-01 | Derma | 453.6 g | — | — | FDA listed | — |
| Zinc Oxide 200 mg/g 67777-0223-02 | Dynarex | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 20% .2 g/g 68016-0159-02 | Pharmacy | 1 tube | — | — | FDA listed | — |
| dabur 20 g/100g 68747-3040-03 | Dabur | 28 g | — | — | FDA listed | — |
| Zinc Oxide 20% .2 g/g 69396-0021-02 | Trifecta | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 20% .2 g/g 69396-0086-02 | Trifecta | 1 tube | — | — | FDA listed | — |
| zinc oxide 20% 20 g/100g 69452-0450-58 | Bionpharma | 425 g | — | — | FDA listed | — |
| Zinc Oxide 20 g/100gthis 69771-0109-39 | Geri-Gentle | 1 tube | — | — | FDA listed | — |
| CVS Zinc Oxide 200 mg/g 69842-0065-34 | CVS | 1 tube | — | — | FDA listed | — |
| Medpura Zinc Oxide 20% 20 g/100g 71399-0245-02 | Akron | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 20% .2 g/g 83324-0052-01 | Chain | 1 tube | — | — | FDA listed | — |
| Zinc Oxide Pharma 200 mg/g 84387-0001-01 | ALLIED | 56.6 g | — | — | FDA listed | — |
| ElixirZincoCare 20 g/100g 84546-0004-01 | ELIXIR | 1 tube | — | — | FDA listed | — |
| Zinc Oxide Skin Protectant 20 g/100g 87236-0007-16 | Aldermed | 454 g | — | — | FDA listed | — |
| restorsea Rejuvenating Day SPF 30 Broad Spectrum UVA UVB with Vibransea Complex 20 g/100g 57670-0000-00 | RESTORSEA | 1 tube | — | — | FDA listed | — |
| SPF 50 Mineral Sunscreen 20 g/100g 72667-0101-01 | Inspec | 50 g | — | — | FDA listed | — |
| Radically Rejuvenating SPF Day Cream 20 g/100g 54136-0152-52 | Better | 52 g | — | — | FDA listed | — |
| Seriously Soothing SPF Day Cream 20 g/100g 54136-0179-52 | Better | 52 g | — | — | FDA listed | — |
| ATTITUDE Oatmeal Sensitive Natural Mineral Sunscreen Stick Unscented SPF 30 20 g/100g 61649-0100-60 | 9055-7588 | 60 g | — | — | FDA listed | — |
| Attitude Kids Oatmeal sensitive mineral sunscreen unscented SPF 30 20 g/100g 61649-0162-75 | 9055-7588 | 75 g | — | — | FDA listed | — |
| Attitude Oatmeal sensitive mineral sunscreen unscented SPF 30 20 g/100g 61649-0165-15 | 9055-7588 | 150 g | — | — | FDA listed | — |
| Aloe UP SPF 33 Mineral 20 g/100g 61477-0231-01 | Aloe | 30 g | — | — | FDA listed | — |
| Attitude mineral sunscreen orange blossom SPF 30 20 g/100g 61649-0022-15 | 9055-7588 | 150 g | — | — | FDA listed | — |
| Attitude mineral sunscreen unscented SPF 30 20 g/100g 61649-0030-85 | Attitude | 85 g | — | — | Discontinued | — |
| Attitude mineral sunscreen tropical SPF 30 20 g/100g 61649-0031-85 | Attitude | 85 g | — | — | Discontinued | — |
| ATTITUDE Sunly Kids Mineral Sunscreen Stick Unscented SPF 30 20 g/100g 61649-0098-60 | 9055-7588 | 60 g | — | — | FDA listed | — |
| ATTITUDE Sunly Tinted Mineral Sunscreen Face Stick Unscented SPF 30 20 g/100g 61649-0097-20 | 9055-7588 | 20 g | — | — | FDA listed | — |
| All Good Mineral Sport Sunscreen Sunstick SPF 30 20 g/100g 75786-0220-01 | Elemental | 17 g | — | — | FDA listed | — |
| Mackenzies SPF 40 Ocean Safe Sunscreen 20 g/100g 80325-0040-02 | Naturally | 80 g | — | — | FDA listed | — |
| Zinctral 20 g/100g 59088-0627-05 | PureTek | 57 g | — | — | FDA listed | — |
| Aloe Up SPF 50 Mineral 20 g/100g 61477-0234-01 | Aloe | 89 g | — | — | FDA listed | — |
| Aloe Up SPF 50 Kids Mineral 20 g/100g 61477-0236-01 | Aloe | 89 g | — | — | FDA listed | — |
| Attitude mineral sunscreen tropical SPF 30 20 g/100g 61649-0021-15 | 9055-7588 | 150 g | — | — | FDA listed | — |
| ATTITUDE Oceanly Phyto-sun lip balm SPF 30 Terracotta 20 g/100g 61649-0046-08 | 9055-7588 | 8.5 g | — | — | FDA listed | — |
| ATTITUDE Sunly Mineral Sunscreen Stick Unscented SPF 30 20 g/100g 61649-0090-60 | 9055-7588 | 60 g | — | — | FDA listed | — |
| ATTITUDE Sunly Mineral Sunscreen Stick Orange Blossom SPF 30 20 g/100g 61649-0092-60 | 9055-7588 | 60 g | — | — | FDA listed | — |
| Attitude Kids mineral sunscreen unscented SPF 30 20 g/100g 61649-0160-15 | 9055-7588 | 150 g | — | — | FDA listed | — |
| Mineral Defense Sport Ceramide Spf-30 20 g/100g 73054-0108-11 | SOLARA | 1 applicator | — | — | FDA listed | — |
| Attitude Kids mineral sunscreen unscented SPF 30 20 g/100g 61649-0038-85 | Attitude | 85 g | — | — | Discontinued | — |
| Attitude tinted mineral sunscreen face unscented SPF 30 20 g/100g 61649-0041-30 | Attitude | 30 g | — | — | Discontinued | — |
| ATTITUDE Oatmeal Sensitive Natural Mineral Sunscreen Face Stick Unscented SPF 30 20 g/100g 61649-0101-20 | 9055-7588 | 20 g | — | — | FDA listed | — |
| All Good Coconut Mineral Sunscreen Sunstick SPF 30 20 g/100g 75786-0221-01 | Elemental | 17 g | — | — | FDA listed | — |
| ATTITUDE Sunly Mineral Sunscreen Face Stick Unscented SPF 30 20 g/100g 61649-0094-20 | 9055-7588 | 20 g | — | — | FDA listed | — |
| Medpride 20 g/100g 52410-3040-03 | Shield | 28 g | — | — | FDA listed | — |
| Medline 20 g/100g 53329-0220-07 | Medline | 14 g | — | — | FDA listed | — |
| ATTITUDE Sunly Mineral Sunscreen Stick Tropical SPF 30 20 g/100g 61649-0091-60 | 9055-7588 | 60 g | — | — | FDA listed | — |
| Bio Spectra Attitude 20 g/100g 61649-0120-01 | 9055-7588 | 75 g | — | — | FDA listed | — |
| BLDG Active Skin Repair Sun Stick Performance Sunscreen 20 g/100g 70489-1423-01 | Innovacyn, | 15 g | — | — | FDA listed | — |
| Stream2Sea SPF 50 20 g/100g 69555-0050-01 | Stream2Sea | 1 jar | — | — | FDA listed | — |
| Stream2Sea Sport Lip Balm SPF 50 20 g/100g 69555-0500-01 | Stream2Sea, | 4 g | — | — | FDA listed | — |
| ATTITUDE Sunly Kids Mineral Sunscreen Face Stick Unscented SPF 30 20 g/100g 61649-0099-20 | 9055-7588 | 20 g | — | — | FDA listed | — |
| Bio Spectra Attitude 20 g/100g 61649-0110-15 | 9055-7588 | 150 g | — | — | FDA listed | — |
| New Kid on the Block 20 g/100g 84568-0552-12 | Dimples | 106.8 g | — | — | FDA listed | — |
| Lasso Tallow Sunscreen Spf 50 20 g/100g 87761-0004-01 | Moes | 140 g | — | — | FDA listed | — |
| ATTITUDE Oceanly Phyto-sun lip balm SPF 30 Baby Rose 20 g/100g 61649-0045-08 | 9055-7588 | 8.5 g | — | — | FDA listed | — |
| ATTITUDE Oceanly Phyto-sun lip balm SPF 30 Peachy Shell 20 g/100g 61649-0047-08 | 9055-7588 | 8.5 g | — | — | FDA listed | — |
| Stream2Sea Reef Safer Mineral Sunscreen SPF40 20 g/100g 69555-0400-10 | Stream2Sea, | 1 jar | — | — | FDA listed | — |
| 365 Whole Foods Market Sport Mineral Spf 30 20 g/100g 42681-0062-01 | Whole | 44 g | — | — | FDA listed | — |
| Stream2Sea Ecostock SPF 40 Sunscreen 20 g/100g 69555-0401-01 | Stream2Sea, | 14 g | — | — | FDA listed | — |
| Utu Broad Spectrum SPF 30 Moisturizing Body Sunscreen 20 g/100g 87952-0004-02 | Utu | 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
🏛️
2017
On the market since
Jan 2017
📍
2026
Currently FDA-listed
9 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 — the ingredient across all brands.
Top reported reactions
Reporter sex
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 69771-0109-38 | 1 TUBE in 1 BOX (69771-109-38) / 28.4 g in 1 TUBE | 2017-01-15 | Active |
| 69771-0109-39 You're viewing this | 1 TUBE in 1 BOX (69771-109-39) / 56.8 g in 1 TUBE | 2017-01-15 | Active |
Pack size FAQ
What quantity is in NDC 69771-0109-39?
NDC 69771-0109-39 contains 1 tube — 1 tube in 1 box / 56.8 g in 1 tube.
What is the difference between NDC 69771-0109-39 and NDC 69771-0109-38?
Both are Zinc Oxide 20 g/100g Ointment — the drug itself is identical. NDC 69771-0109-39 is the 1 tube package, while NDC 69771-0109-38 is the 1 tube package.
What NDC number is used to bill for this package of Zinc Oxide 20 g/100g Ointment?
Bill NDC 69771-0109-39 — the 11-digit billing format is 69771010939. 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 69771-109-39, 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: 69771-0109-39, written without dashes as 69771010939. 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 69771-0109-39, the first segment (69771) is the labeler code FDA assigned to Geri-Gentle Corporation; the middle segment (0109) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (39) 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 Geri-Gentle Corporation. 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 1 tube (69771-0109-38). 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?
Geri-Gentle Corporation 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 ▾
Uses helps treat and prevent diaper rash dries the oozing and weeping of: poison ivy poison oak poison sumac
⏱️ Dosage and Administration ▾
Directions for Diaper Rash change wet and soiled diaper promptly cleanse the diaper area and allow to dry apply as needed
⚠️ Warnings ▾
Warnings For external use only When using this product do not get into eyes do not use over large area of the body Stop Use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again in a few days if you are allergic to any of these ingredients Do not use on deep puncture wounds animal bites serious burns Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
📦 Storage and Handling ▾
Other information store at 59°-86°F (15°-30°C) avoid excessive heat
🧪 Active Ingredient ▾
Active ingredient Zinc Oxide (20%w/w)
🧪 Inactive Ingredients ▾
Inactive Ingredients Cetostearyl Alcohol, Cetomacrogol 1000, Lanolin, Light Liquid Paraffin, White Soft Paraffin
🎯 Purpose ▾
Purpose Skin Protectant
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.