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Vitamin A D Lanolin, Petrolatum 155 mg/g; 534 mg/g Ointment — NDC 41250-0091-26 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vitamin A D Lanolin, Petrolatum 155 mg/g; 534 mg/g Ointment — NDC 41250-091-26 (Billing 41250-0091-26)

by Meijer, Inc. · 1 TUBE in 1 CARTON / 113 g in 1 TUBE

This is a package of Vitamin A D Lanolin, Petrolatum 155 mg/g; 534 mg/g Ointment from Meijer, Inc., marketed since Apr 2008 and currently FDA-listed. It is this product's only package size.

NDC 41250-0091-26
🏷️ FDA NDC (as labeled) 41250-091-26 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 41250-091-26 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41250 labeler · 091 product · 26 package
Package marketed since
Apr 8, 2008
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 4125009126 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-091-26
Product NDC 41250-091
11-digit billing NDC 41250009126
RxCUI 664981
UNII 7EV65EAW6H, 4T6H12BN9U
Application # M016
SPL Set ID adc3bb9b-ed8a-4b65-b44c-1d1e978c89ec
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-04-08
Route TOPICAL
Dosage form OINTMENT
Substance LANOLIN; PETROLATUM
Quick answers
  • RxCUI (RxNorm): 664981
Why two NDCs? The FDA registers this code as 41250-091-26 — 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 → 41250-0091-26. 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.

Clinical

🧪 What is this product?

This is an over-the-counter topical ointment containing lanolin and petrolatum as active ingredients. Both are occlusive moisturizers that are typically used to help soften and protect dry skin, minor wounds, and chapped or irritated areas when applied directly to the skin. As an OTC monograph product, it is marketed under established FDA guidelines for skin protectant ointments rather than through individual product approval. The greasy base helps seal in moisture and create a barrier against further irritation.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.
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
41250-0091-26 You're viewing this Main listing 1 TUBE in 1 CARTON / 113 g in 1 TUBE 2008-04-08 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
LDR Vitamans A and D 53.4 g/100g; 15.5 g/100g 70000-0358-01 Cardinal 425 g $0.013 — Availability likely —
Walgreens Vitamin A and D skin protectant 53.4 g/100g; 15.5 g/100g 00363-0582-26 Walgreen 1 tube — — FDA listed —
First Aid A and D 15.5 g/100g; 53.4 g/100g 00363-5362-07 Walgreen 1 tube — — FDA listed —
Baby Vitamin A and D 15.5 g/100g; 53.4 g/100g 00363-6253-07 Walgreen 1 tube — — FDA listed —
Target Vitamin A and D Diaper Rash 534 mg/g; 155 mg/g 11673-0721-40 Target 1 tube — — FDA listed —
Lanolin, Petrolatum 155 mg/g; 534 mg/g 11822-0103-04 Rite 1 tube — — FDA listed —
Skin Protectant for Babies and kids 155 mg/g; 534 mg/g 13709-0352-01 Neilmed 1 tube — — FDA listed —
Vitamin A D 155 mg/g; 534 mg/g 30142-0022-26 Kroger 1 tube — — FDA listed —
Jell with Vitamin A D 53.4 g/100g; 15.5 g/100g 30400-0215-10 Jell 1 tube — — FDA listed —
Vitamin A D 155 mg/g; 534 mg/g 36800-0017-26 Topco 1 tube — — FDA listed —
Vitamin A D 155 mg/g; 534 mg/gthis 41250-0091-26 Meijer, 1 tube — — FDA listed —
CVS Health Vitamin A and D Skin Protectant 155 mg/g; 534 mg/g 51316-0399-01 CVS 454 g — — FDA listed —
Kidgets Baby Petroleum Jelly with Vitamin A D 53.4 g/100g; 15.5 g/100g 51628-4248-01 MY 113 g — — FDA listed —
Vitamin A and D 15.5 g/100g; 53.4 g/100g 55319-0103-01 Family 113 g — — FDA listed —
Vitamin A and D 53.4 g/100g; 15.5 g/100g 55319-0603-01 MIDWOOD 113 g — — FDA listed —
Gentle STEPS vitamins A and D Diaper Rash and Skin Protectant 15.5 g/100g; 53.4 g/100g 55910-0805-72 Old 1 tube — — FDA listed —
Multi-Purpose Skin Protectant 53.4 g/100g; 15.5 g/100g 59779-0841-03 CVS 1 tube — — FDA listed —
AD First Aid Multipurpose 53.4 g/100g; 15.5 g/100g 65197-0400-10 WellSpring 1 tube — — FDA listed —
AD PREVENT Original 15.5 g/100g; 53.4 g/100g 65197-0401-00 WellSpring 454 g — — FDA listed —
AD Anti-Chafing 15.5 g/100g; 53.4 g/100g 65197-0408-15 WellSpring 1 tube — — FDA listed —
AD Skin Protectant 15.5 g/100g; 53.4 g/100g 65197-0470-16 WellSpring 454 g — — FDA listed —
FDS intimate Whole Body Medicated Chafing 15.5 g/100g; 53.4 g/100g 65197-0730-15 WellSpring 1 tube — — FDA listed —
A and D Diaper Rash and Skin Protectant .15 mg/g; .53 mg/g 67234-0030-01 Natureplex 1 tube — — FDA listed —
Vitamin A and D 53.4 g/100g; 15.5 g/100g 69396-0009-20 Trifecta 1 tube — — FDA listed —
Vitamin A and D 15.5 g/100g; 53.4 g/100g 69396-0018-05 Trifecta 1 tube — — FDA listed —
Lanolin, Petrolatum 155 mg/g; 534 mg/g 69842-0488-26 CVS 1 tube — — FDA listed —
TheraCare A and D 15.5 g/100g; 53.4 g/100g 71101-0013-01 Veridian 1 tube — — FDA listed —
mama bear DIAPER RASH Skin Protectant 155 mg/g; 534 mg/g 72288-0342-01 AMAZON.COM 454 g — — FDA listed —
Vitamin A D 534 mg/g; 155 mg/g 79903-0328-04 Walmart 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

🏛️
2008
On the market since
Apr 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.

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 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 GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII 5K47SSQ51G
    A fragrant compound found in plants like lavender and bergamot. It's used as a flavoring and aroma agent to improve the taste and smell of medications.
  • UNII XOF597Q3KY
    A refined form of wax made from petroleum, microcrystalline wax is used in medicines as a coating agent, binder, and hardening ingredient. It helps give tablets and capsules their shape and protective outer layer.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII R53Q4ZWC99
    Terpineol is a fragrant alcohol derived from pine oil or other plant sources. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.

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

The official label also statescod liver oil, fragrance, limonene, linalool, linalyl acetate, microcrystalline wax, mineral oil, paraffin, terpineol

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

LabelerMeijer, Inc.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedApr 2008
Product typeHuman Otc Drug
Portfolio202 products on file

More NDCs from Meijer, Inc. labeler code 41250

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 🤒 Adverse Reactions 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 38 words ▾

Uses helps treat and prevent diaper rash temporarily protects minor: cuts - scrapes - burns temporarily protects and helps relieve chafed, chapped or cracked skin and lips helps protect from the drying effects of wind and cold weather

⏱️ Dosage and Administration 50 words ▾

Directions for skin protectant use: apply as needed for diaper rash use: change wet or 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 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 26 words ▾

Adverse Reactions OUR QUALITY GUARANTEE The Meijer Family www.meijer.com/satisfaction Questions? 1-888-593-0593 DISTRIBUTED BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com PAPER BOX METAL TUBE how2recycle.info

📦 Storage and Handling 10 words ▾

Other information store between 20º and 25ºC (68º and 77ºF)

🧪 Active Ingredient 6 words ▾

Active ingredients Lanolin 15.5% Petrolatum 53.4%

🧪 Inactive Ingredients 16 words ▾

Inactive ingredients cod liver oil, fragrance, limonene, linalool, linalyl acetate, microcrystalline wax, mineral oil, paraffin, terpineol

🎯 Purpose 3 words ▾

Purpose Skin protectant

📄 Do Not Use 12 words ▾

Do not use on deep or puncture wounds animal bites serious burns

📄 When Using This Product 9 words ▾

When using this product do not get into eyes

📄 Stop Use and Ask a Doctor If 25 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 19 words ▾

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

📄 Package Label / Principal Display Panel 45 words ▾

Principal Display Panel NDC 41250-091-26 meijer ® Compare to A+D ® Original Ointment* vitamin A & D ointment Diaper Rash Ointment & Skin Protectant Helps heal dry, chafed skin Protects & soothes minor cuts & burns HYPOALLERGENIC NET WT. 4 OZ (113 g) image description

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 Meijer, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Meijer, 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.
← 41250-0082-00 · Meijer 41250-0098-53 · Meijer →
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.