Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Diaper Rash ZINC OXIDE 400 mg/g Paste, 1 tube — NDC 11673-020-26 (Billing 11673-0020-26)
by Target Corporation · 1 TUBE in 1 PACKAGE / 113.3 g in 1 TUBE
This is a package of 1 tube of Diaper Rash ZINC OXIDE 400 mg/g Paste from Target Corporation, no longer marketed (first marketed Mar 2008), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.
NDC 11673-0020-26
🏷️ FDA NDC (as labeled)
11673-020-26
billing pads the product segment with a zero
This package
Contains1 tube
Pack sizes2 compare ↓
Main listing for product 11673-020 · Also comes in:
453.5 g 11673-020-43
🗂️ 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 →
⚠️
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 ↗
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
11673-020-26
Product NDC
11673-020
11-digit billing NDC
11673002026
RxCUI
1094560
UNII
SOI2LOH54Z
Application #
M016
SPL Set ID
7fb5f9ca-cd90-4933-9fe8-907ece00458b
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2008-03-24
Route
TOPICAL
Dosage form
PASTE
Substance
ZINC OXIDE
Quick answers
- RxCUI (RxNorm): 1094560
Why two NDCs?
The FDA registers this code as 11673-020-26 — 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 → 11673-0020-26. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
🧪 What is this product?
This is an over-the-counter topical paste containing zinc oxide, marketed under the FDA's established rules for diaper rash products. Zinc oxide is commonly used in skin-care products as a protective barrier and is included in many formulations meant to soothe and protect irritated skin. This paste form is applied directly to affected skin areas. As an OTC monograph drug, it follows a standard FDA category for products of this type rather than being individually approved through a separate application.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about ZINC OXIDE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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:
453.5 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 11673-0020-26 You're viewing this Main listing | 1 TUBE in 1 PACKAGE / 113.3 g in 1 TUBE | 2008-03-24 | — | Discontinued by firm |
| 11673-0020-43 11673-020-43 | 1 TUBE in 1 PACKAGE / 453.5 g in 1 TUBE | 2008-03-24 | — | Active |
Pack size FAQ
What quantity is in this package?
This package contains 1 tube — 1 tube in 1 package / 113.3 g in 1 tube.
How does this package differ from NDC 11673-0020-43?
Both are Diaper Rash ZINC OXIDE 400 mg/g Paste — the drug itself is identical. This page's package is the 1 tube one, while NDC 11673-0020-43 is the 1 tube package.
What NDC number is used to bill for this package of Diaper Rash ZINC OXIDE 400 mg/g Paste?
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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Zinc Oxide 400 mg/g 00363-1020-26 | Walgreen | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 11344-0020-26 | Nice-Pak | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/gthis 11673-0020-26 | Target | 1 tube | — | — | Discontinued | — |
| Target Maximum Strength Zinc Oxide Diaper Rash 400 mg/g 11673-0728-40 | Target | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 37808-0020-26 | H | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 41250-0412-26 | Meijer, | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 55910-0020-26 | Old | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 400 mg/g 69842-0468-26 | CVS | 1 tube | — | — | FDA listed | — |
| Desitin Maximum Strength Diaper Rash 400 mg/g 69968-0061-01 | Kenvue | 1 tube | — | — | FDA listed | — |
| Desitin Maximum Strength Zinc Oxide Diaper Rash 400 mg/g 69968-0396-01 | Kenvue | 454 g | — | — | FDA listed | — |
| Desitin Maximum Strength Zinc Oxide Diaper Rash 400 mg/g 69968-0768-01 | Kenvue | 1 tube | — | — | FDA listed | — |
| Desitin Maximum Strength Zinc Oxide Diaper Rash 400 mg/g 69968-0848-01 | Kenvue | 454 g | — | — | FDA listed | — |
| CVS Health Diaper Rash 400 mg/g 69842-0058-20 | CVS | 1 tube | — | — | FDA listed | — |
| Dr. Sheffield Diaper Rash 400 mg/g 11527-0058-40 | Sheffield | 1 tube | — | — | FDA listed | — |
| Natureplex Diaper Rash 400 mg/g 67234-0001-01 | Natureplex | 1 tube | — | — | FDA listed | — |
| Walgreens Maximum Diaper Rash 400 mg/g 00363-7280-20 | Walgreens | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 49035-0952-26 | Walmart | 1 tube | — | — | FDA listed | — |
| Baby Diaper Rash Cream 400 mg/g 73418-0301-01 | Hello | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 67091-0020-26 | WinCo | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 36800-0020-26 | Topco | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 41163-0020-26 | United | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 400 mg/g 72288-0989-26 | Amazon.com | 1 tube | — | — | FDA listed | — |
| Diaper Rash 400 mg/g 30142-0020-26 | The | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 400 mg/g 11822-0534-01 | Rite | 1 tube | — | — | FDA listed | — |
| Vitacilina Bebe Diaper Rash 400 mg/g 81929-0002-01 | Taisho | 1 tube | — | — | FDA listed | — |
| Zinc Oxide 400 mg/g 72476-0920-26 | ADUSA | 1 tube | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2008
On the market since
Mar 2008
📍
2026
Currently FDA-listed
18 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.
- FDA Orange Book · refreshed Sep 3, 2026
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 BBL281NWFG
Cod liver oil is a natural oil derived from fish liver that serves as a source of omega-3 fatty acids and vitamins A and D in formulations. It's used as a nutrient supplement ingredient and as an emollient to help soften and smooth the product.
-
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 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 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.
-
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 O8232NY3SJ
A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
-
UNII 2ZA36H0S2V
Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
8 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statespetrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerTarget Corporation
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedMar 2008
Product typeHuman Otc Drug
Portfolio409 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
🤒 Adverse Reactions
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 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 ▾
Uses • helps treat and prevent diaper rash • protects chafed skin due to the diaper rash and helps seal out wetness
⏱️ Dosage and Administration ▾
Directions change wet and soiled diapers promptly cleanse the diaper area allow to dry apply ointment liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged
⚠️ Warnings ▾
Warnings For external use only
🤒 Adverse Reactions ▾
Adverse Reactions Distributed by Target Corporation Minneapolis, MN 55403 TM & © 2025 Target Brands, Inc. Not tested on animals
📦 Storage and Handling ▾
Other information • store between 20⁰ and 25⁰C (68⁰ and 77⁰F)
🧪 Active Ingredient ▾
Active ingredient Zinc oxide 40%
🧪 Inactive Ingredients ▾
Inactive ingredients petrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance
🎯 Purpose ▾
Purpose Skin Protectant
📄 When Using This Product ▾
When using this product do not get into eyes
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions Call 1-800-910-6874
📄 Package Label / Principal Display Panel ▾
Principal display panel Compare to Desitin ® Maximum Strength 40% Zinc Oxide Diaper Rash Paste* Maximum Strength Diaper Rash Paste 40% Zinc Oxide Skin Protectant Protects chafed skin and seals out wetness Made without parabens or phthalates Helps Treat & Prevent Diaper Rash Pediatrician Tested Hypoallergenic up & up™ NET WT 16 OZ (454 g) image description
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 ↗
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 Diaper Rash (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 37%
Female · 63%
Unknown · 0%
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.
About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 tube (11673-0020-43). 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?
Target 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.
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.