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Burts Bees Baby Bee Diaper Rash Zinc Oxide 40 g/100g Ointment — NDC 26052-0028-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Burts Bees Baby Bee Diaper Rash Zinc Oxide 40 g/100g Ointment — NDC 26052-028-02 (Billing 26052-0028-02)

by BURT'S BEES, INC. · 1 TUBE in 1 CARTON / 85 g in 1 TUBE

This is a package of Burts Bees Baby Bee Diaper Rash Zinc Oxide 40 g/100g Ointment from BURT'S BEES, INC., marketed since May 2015 and currently FDA-listed.

NDC 26052-0028-02
🏷️ FDA NDC (as labeled) 26052-028-02 billing pads the product segment with a zero
This package
Contains85 g in 1 tube Pack sizes2 compare ↓
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 →

NDC database record

One package, one record: these facts belong to NDC 26052-028-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
26052 labeler · 028 product · 02 package
Package marketed since
May 29, 2015
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 2605202802 2
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) 26052-028-02
Product NDC 26052-028
11-digit billing NDC 26052002802
RxCUI 244638
UNII SOI2LOH54Z
Application # part347
SPL Set ID 168b31b1-9260-61f8-e054-00144ff8d46c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH FINAL
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-05-29
Route TOPICAL
Dosage form OINTMENT
Substance ZINC OXIDE
Quick answers
  • RxCUI (RxNorm): 244638
Why two NDCs? The FDA registers this code as 26052-028-02 — 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 → 26052-0028-02. 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 topical ointment containing zinc oxide, marketed for diaper rash. Zinc oxide is commonly used in skin barrier products applied directly to the skin to help protect against moisture and irritation. This product is an OTC monograph drug, meaning it follows FDA's established safety and use guidelines for this category rather than undergoing individual drug approval review.

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.

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: 85 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
26052-0028-01 26052-028-01 Main listing 85 g in 1 TUBE 2015-05-29 — Active
26052-0028-02 You're viewing this 1 TUBE in 1 CARTON / 85 g in 1 TUBE 2015-05-29 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 carton / 85 g in 1 tube.
What NDC number is used to bill for this package of Burts Bees Baby Bee Diaper Rash Zinc Oxide 40 g/100g Ointment?
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
Zinc Oxide 40% 40 g/100g 70000-0469-01 Cardinal 1 tube $0.034 — Availability likely —
Dr. Sheffield Diaper Rash 400 mg/g 11527-0058-40 Sheffield 1 tube — — FDA listed —
Zinc Oxide 400 mg/g 11822-0534-01 Rite 1 tube — — FDA listed —
Burts Bees Baby Bee Diaper Rash 40 g/100gthis 26052-0028-02 BURT'S 1 tube — — FDA listed —
Diaper Rash 400 mg/g 30142-0020-26 The 1 tube — — FDA listed —
Diaper Rash 400 mg/g 41163-0020-26 United 1 tube — — FDA listed —
Diaper Rash 400 mg/g 49035-0952-26 Walmart 1 tube — — FDA listed —
Diaper Rash 400 mg/g 67091-0020-26 WinCo 1 tube — — FDA listed —
Natureplex Diaper Rash 400 mg/g 67234-0001-01 Natureplex 1 tube — — FDA listed —
DiaperRashOintment 40 g/100g 68016-0128-20 Pharmacy 113 g — — FDA listed —
Best Choice Diaper Rash 40 g/100g 69396-0152-01 Trifecta 113 g — — FDA listed —
CVS Health Diaper Rash 400 mg/g 69842-0058-20 CVS 1 tube — — FDA listed —
Zinc Oxide 400 mg/g 72288-0989-26 Amazon.com 1 tube — — FDA listed —
Vitacilina Bebe Diaper Rash 400 mg/g 81929-0002-01 Taisho 1 tube — — FDA listed —
Quality Choice Diaper Rash 40 g/100g 83324-0042-01 Chain 113 g — — FDA listed —
Diaper Rash 40 g/100g 87236-0018-04 Aldermed 113 g — — FDA listed —
Triple 3x Max Diaper Rash 40 g/100g 16864-0061-01 Advantice 1 tube — — FDA listed —
Diaper Rash Cream 2oz 40 g/100g 57337-0164-01 Rejoice 1 tube — — FDA listed —
Diaper Rash Cream 40% ZINC 40 g/100g 77338-0164-01 ASTONEA 1 tube — — FDA listed —
Diaper Rash Cream 2.5oz 40 g/100g 57337-0165-01 Rejoice 1 tube — — FDA listed —
Diaper Rash Cream 5.6oz 40 g/100g 57337-0170-01 Rejoice 160 g — — FDA listed —
Aquaphor Healing Fast Relief Diaper Rash 40 g/100g 10356-0115-10 Beiersdorf 99 g — — FDA listed —
Diaper Rash Cream 5.6oz 40 g/100g 58503-0202-01 China 160 g — — FDA listed —
Diaper Rash Cream 15oz 40 g/100g 58503-0205-01 China 425 g — — FDA listed —
Diaper Rash Cream 15oz 40 g/100g 57337-0169-01 Rejoice 425 g — — FDA listed —
Earth Baby Diaper Rash Cream 40 g/100g 62588-0904-02 Earth 1 tube — — FDA listed —
Drs. Pharmacy Baby Healing 40 g/100g 80489-0904-01 OL 50 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

🏛️
2015
On the market since
May 2015
📍
2026
Currently FDA-listed
11 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 66YXD4DKO9
    A natural oil extracted from almond kernels. It's used in medicines as an emollient and solvent to help dissolve or suspend active ingredients and improve texture in topical and oral formulations.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 331KBJ17RK
    Canola oil is a plant-based oil derived from rapeseed. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and may improve how the body absorbs certain medications.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII UB27587839
    A plant-derived oil from Roman chamomile flowers. It's used in medicines as a flavoring agent and fragrance to improve taste and smell.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • 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 9RES347CKG
    A fragrant oil derived from lavandin plants, used as a flavoring and aromatic agent to improve the taste and smell of medicines.
  • UNII 19AH1RAF4M
    A plant extract from lavender flowers used as a flavoring and fragrance agent in medicines. It adds taste and aroma to make the product more pleasant to take.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • 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 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.

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

The official label also statesPRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL, BEESWAX, LANOLIN, RICINUS COMMUNIS (CASTOR) SEED OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, GLYCERYL ROSINATE, OLEA EUROPAEA (OLIVE) FRUIT OIL, HYDROGENATED CASTOR OIL, OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES, ANTHEMIS NOBILIS FLOWER OIL, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER, LAVANDULA HYBRIDA OIL, CALENDULA OFFICINALIS FLOWER EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, TOCOPHEROL, GLYCINE SOJA (SOYBEAN) OIL, CANOLA OIL

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

LabelerBURT'S BEES, INC.
FDA applicationpart347 (OTC MONOGRAPH FINAL)
Labeler code26052
First marketedMay 2015
Product typeHuman Otc Drug
Portfolio6 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage 19 words ▾

USES Helps treat and prevent diaper rash Protects chafed skin due to diaper rash and helps seal out wetness

⏱️ Dosage and Administration 39 words ▾

DIRECTIONS CHANGE WET AND SOILED DIAPERS PROMPTLY. CLEANSE THE DIAPER AREA AND 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 12 words ▾

For external use only. When using this product keep out of eyes.

📦 Storage and Handling 6 words ▾

OTHER INFORMATION STORE AT ROOM TEMPERATURE

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENT Zinc Oxide 40%

🧪 Inactive Ingredients 66 words ▾

INACTIVE INGREDIENTS PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL, BEESWAX, LANOLIN, RICINUS COMMUNIS (CASTOR) SEED OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, GLYCERYL ROSINATE, OLEA EUROPAEA (OLIVE) FRUIT OIL, HYDROGENATED CASTOR OIL, OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES, ANTHEMIS NOBILIS FLOWER OIL, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER, LAVANDULA HYBRIDA OIL, CALENDULA OFFICINALIS FLOWER EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, TOCOPHEROL, GLYCINE SOJA (SOYBEAN) OIL, CANOLA OIL

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Stop Use and Ask a Doctor If 16 words ▾

Stop use and ask a doctor if condition worstened or does not improve after 7 days

📄 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.

📄 Package Label / Principal Display Panel 32 words ▾

MAXIMUM STRENGTH - 40% ZINC OXIDE BURT'S BEES BABY BEE DIAPER RASH OINTMENT HELPS TREAT & PREVENT DIAPER RASH 100% NATURAL NET WT. 3 oz. / 85 g Baby Bee Diaper Ointment

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 Final". 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 BURT'S BEES, 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 85 g (26052-0028-01). 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?
BURT'S BEES, 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.
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.