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Everyday Diaper Rash Cream Zinc Oxide 14 g/100g Cream, 1 tube — NDC 69366-0507-17 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Everyday Diaper Rash Cream Zinc Oxide 14 g/100g Cream, 1 tube — NDC 69366-507-17 (Billing 69366-0507-17)

by The Honest Company, Inc · 1 TUBE in 1 CARTON / 70.8 g in 1 TUBE

This is a package of 1 tube of Everyday Diaper Rash Cream Zinc Oxide 14 g/100g Cream from The Honest Company, Inc, marketed since Apr 2023 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 69366-0507-17
🏷️ FDA NDC (as labeled) 69366-507-17 billing pads the product segment with a zero
This package
Contains1 tube Pack sizes2 compare ↓
Main listing for product 69366-507 · Also comes in: 170 g 69366-507-33
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 69366-507-17 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69366 labeler · 507 product · 17 package
Package marketed since
Apr 17, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0817810014567
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) 69366-507-17
Product NDC 69366-507
11-digit billing NDC 69366050717
RxCUI 1546589
UNII SOI2LOH54Z
UPC 0817810014567
Application # M016
SPL Set ID dfdc5021-9551-3867-e053-2995a90af52b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-04-17
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE
Quick answers
  • RxCUI (RxNorm): 1546589
Why two NDCs? The FDA registers this code as 69366-507-17 — 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 → 69366-0507-17. 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 diaper rash cream containing zinc oxide as its active ingredient. Zinc oxide is commonly used in topical products to help protect and soothe irritated skin. The cream is applied directly to the affected skin area and functions as a barrier to help reduce moisture and friction. This product is marketed under the FDA's monograph rules for over-the-counter diaper rash treatments.

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: 170 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
69366-0507-17 You're viewing this Main listing 1 TUBE in 1 CARTON / 70.8 g in 1 TUBE 2023-04-17 — Active
69366-0507-33 69366-507-33 170 g in 1 TUBE 2024-01-21 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1 tube — 1 tube in 1 carton / 70.8 g in 1 tube.
How does this package differ from NDC 69366-0507-33?
Both are Everyday Diaper Rash Cream Zinc Oxide 14 g/100g Cream — the drug itself is identical. This page's package is the 1 tube one, while NDC 69366-0507-33 is the 170 g package.
What NDC number is used to bill for this package of Everyday Diaper Rash Cream Zinc Oxide 14 g/100g Cream?
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
BabyDiaperCream 14 g/100g 42681-0032-01 Whole 114 g — — FDA listed —
Everyday Diaper Rash Cream 14 g/100gthis 69366-0507-17 The 1 tube — — FDA listed —
Seedlings Diaper Rash Cream 140 mg/g 70631-0039-57 Young 1 tube — — FDA listed —
Pipette Diaper Rash 14 g/100mL 73517-0427-02 Amyris, 1 tube — — FDA listed —
Doctors Diaper Rash Cream 140 mg/g 83432-0402-00 DOCTOR'S 56.7 g — — FDA listed —
Pipette Diaper Rash 14 g/100mL 84723-0007-02 Pipette 1 tube — — FDA listed —
Beyond Good Diaper Rash 140 mg/g 87676-0001-01 Babylist, 113 g — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 7 14 g/100g 84435-0107-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 2 14 g/100g 84435-0102-02 G2G 1 tube — — FDA listed —
OS-01 Body SPF 30 14 g/100g 62742-4264-02 Allure 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 3 14 g/100g 84435-0103-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 6 14 g/100g 84435-0106-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 4 14 g/100g 84435-0104-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 1 14 g/100g 84435-0101-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 5 14 g/100g 84435-0105-02 G2G 1 tube — — FDA listed —
Counter Beauty Dew Skin Tinted Moisturizer No. 8 14 g/100g 84435-0108-02 G2G 1 tube — — FDA listed —
OS-01 Body SPF 30 14 g/100g 84451-0001-02 ONESKIN, 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.

Availability & generic status

🏛️
2023
On the market since
Apr 2023
📍
2026
Currently FDA-listed
3 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 6L246LAM9T
    A synthetic oil derived from glycerol and adipic acid. It acts as an emulsifier and solubilizer in medicines, helping mix ingredients that don't naturally blend together and improving how the body absorbs the active drug.
  • UNII R8WTH25YS2
    Glyceryl dibehenate is a wax-like substance made from behenate fatty acids and glycerol. It functions as a binder and release-control agent in tablets and capsules, helping hold ingredients together and regulate how quickly the medicine dissolves and releases in your body.
  • UNII 42DG15CHXV
    A natural plant wax derived from sunflower seeds. It serves as a lubricant and glidant to help powders flow smoothly during manufacturing and tablet formation.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII 9KJL21T0QJ
    Linoleic acid is an omega-6 fatty acid derived from plant oils. It serves as an emulsifier and skin conditioning agent in topical formulations, helping ingredients mix smoothly and improving product texture.
  • 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 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 PL360EPO9J
    Soy sterol is a plant-derived fat extracted from soybeans. It's used as an emulsifier and stabilizer to help keep oil and water mixed together and maintain the medicine's texture and consistency.
  • UNII 8I089SAH3T
    A carbohydrate powder extracted from potatoes. It serves as a filler to add bulk and volume to the tablet or capsule, and as a disintegrant to help the medicine break apart and release its active ingredient in your body.
  • UNII 3YYE6VJS0P
    A compound derived from licorice root extract combined with stearyl alcohol. It acts as an emollient and skin-conditioning agent that helps soften and smooth the product's texture while providing a protective barrier on the skin or mucous membranes.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • 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 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.

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

The official label also statesInactive ingredients: Helianthus Annuus (Sunflower) Seed Oil, Bis-Diglyceryl Polyacyladipate-2, Polyhydroxystearic Acid, Glyceryl Behenate, Helianthus Annuus (Sunflower) Seed Wax, Solanum Tuberosum (Potato) Starch, Caprylic/Capric Triglyceride, Linoleic Acid, Phytosterols, Phospholipids, Bisabolol, Zinc Carbonate,Water (Aqua/Eau), Stearyl Glycyrrhetinate, Tocopherol Inactive ingredients: Helianthus Annuus (Sunflower) Seed Oil, Bis-Diglyceryl Polyacyladipate-2, Polyhydroxystearic Acid, Glyceryl Behenate, Helianthus Annuus (Sunflower) Seed Wax, Solanum Tuberosum (Potato) Starch, Caprylic/Capric Triglyceride, Linoleic Acid, Phytosterols, Phospholipids, Bisabolol, Water (Aqua/Eau), Stearyl Glycyrrhetinate, Tocopherol

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

LabelerThe Honest Company, Inc
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code69366
First marketedApr 2023
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from The Honest Company, Inc labeler code 69366

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 📄 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 19 words ▾

Uses: Helps treat and prevent diaper rash Protects chafed skin due to diaper rash and helps seal out wetness.

⏱️ Dosage and Administration 48 words ▾

Directions: Change soiled and wet diapers promptly, cleanse the diaper area, and allow to dry Apply diaper rash cream liberally as often as necessary to help prevent or treat irritation, with each diaper change, and especially at bedtime or anytime when exposure to wet diapers may be prolonged.

⚠️ Warnings 60 words ▾

Warnings: For external use only. When using this product • do not get into eyes. 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. If swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 5 words ▾

Active ingredient Zinc Oxide 14%

🧪 Inactive Ingredients 69 words ▾

Inactive ingredients: Helianthus Annuus (Sunflower) Seed Oil, Bis-Diglyceryl Polyacyladipate-2, Polyhydroxystearic Acid, Glyceryl Behenate, Helianthus Annuus (Sunflower) Seed Wax, Solanum Tuberosum (Potato) Starch, Caprylic/Capric Triglyceride, Linoleic Acid, Phytosterols, Phospholipids, Bisabolol, Zinc Carbonate,Water (Aqua/Eau), Stearyl Glycyrrhetinate, Tocopherol

Inactive ingredients: Helianthus Annuus (Sunflower) Seed Oil, Bis-Diglyceryl Polyacyladipate-2, Polyhydroxystearic Acid, Glyceryl Behenate, Helianthus Annuus (Sunflower) Seed Wax, Solanum Tuberosum (Potato) Starch, Caprylic/Capric Triglyceride, Linoleic Acid, Phytosterols, Phospholipids, Bisabolol, Water (Aqua/Eau), Stearyl Glycyrrhetinate, Tocopherol

🎯 Purpose 3 words ▾

Purpose Skin protectant

📄 When Using This Product 10 words ▾

When using this product • do not get into eyes.

📄 Stop Use and Ask a Doctor If 27 words ▾

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 18 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

📄 Package Label / Principal Display Panel 163 words ▾

HONEST ® EVERYDAY DIAPER RASH CREAM FRAGRANCE FREE Zinc Oxide Skin Protectant + Soothing Phyto-Blend™ Net Wt. 2.5 oz. (70.8 g) © 2022 Distributed by The Honest Company, Inc., 12130 Millennium Dr #500 Los Angeles, CA 90094 HONEST.COM • 888-862-8818 carton 2.5 oz

Tube 6 oz

HONEST ® EVERYDAY DIAPER RASH CREAM FRAGRANCE FREE Zinc Oxide Skin Protectant + Soothing Phyto-Blend™ Net Wt. 2.5 oz. (70.8 g) © 2022 Distributed by The Honest Company, Inc., 12130 Millennium Dr #500 Los Angeles, CA 90094 HONEST.COM Label

HONEST ® EVERYDAY DIAPER RASH CREAM FRAGRANCE FREE Zinc Oxide Skin Protectant + Soothing Phyto-Blend™ Net Wt. 2.5 oz. (70.8 g) © 2022 Distributed by The Honest Company, Inc., 12130 Millennium Dr #500 Los Angeles, CA 90094 HONEST.COM Label

HONEST ® EVERYDAY DIAPER RASH CREAM FRAGRANCE FREE Zinc Oxide Skin Protectant + Soothing Phyto-Blend™ Net Wt. 2.5 oz. (70.8 g) © 2022 Distributed by The Honest Company, Inc., 12130 Millennium Dr #500 Los Angeles, CA 90094 HONEST.COM Label

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 The Honest Company, 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 170 g (69366-0507-33). 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?
The Honest Company, 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.
← 69366-0505-23 · The 69366-0508-29 · The →
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.