NDC 67777-0215-08 — Vitamin A D PETROLATUM 93 g/100g Ointment

🆔 Identity & classification

FDA NDC (as labeled) 67777-215-08

Product NDC 67777-215

11-digit billing NDC 67777021508

NCPDP billing unit GM — per gram (weight)

RxCUI 1440181

UNII 4T6H12BN9U

Application # M016

SPL Set ID db4df818-cb0c-434d-e053-2a95a90aaa19

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2022-03-28

Route TOPICAL

Dosage form OINTMENT

Substance PETROLATUM

GCN Seq No 005440

GCN 21590

HICL code 001077

Ingredient (HICL) Vitamins A And D

HIC1 code L

Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue

HIC2 code L2

Therapeutic class — intermediate (HIC2) Emollients

HIC3 code L2A

Therapeutic class — specific (HIC3) Emollients

AHFS code 84:24.12.00

AHFS class Basic Ointments And Protectants

FDB label name VITAMIN A AND D OINTMENT PKT

FDB brand name Vitamin A And D

Legend status O — Over-the-counter (OTC) drug or device

Why two NDCs? The FDA registers this code as 67777-215-08 — 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 → 67777-0215-08. 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

LabelerDynarex Corporation

FDA applicationM016 (OTC MONOGRAPH DRUG)

Labeler code67777

First marketedMar 2022

Product typeHuman Otc Drug

Portfolio60 products on file

🔎 All NDCs from Dynarex Corporation

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

Label name VITAMIN A AND D OINTMENT PKT Ingredient Vitamins A And D

🧪 What is this product?

This is a topical ointment marketed as an over-the-counter monograph drug. The active ingredient is petrolatum, a mineral oil-based lubricant commonly used in skin care products to help soften and protect the skin. Petrolatum-based ointments are typically applied to the skin to soothe dryness and create a protective barrier.

Patient education

📘 MedlinePlus patient leaflet ↗

Supplement & herbal interactions

Some supplements/herbs that may interact with Petrolatum — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor

🌿 Every supplement checked against Petrolatum (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.

💊 What it looks like

ShapeFreeform

One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.

Where does this data come from?

Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 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 1D1K0N0VVC
A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
UNII 9VU1KI44GP
Vitamin D is a fat-soluble nutrient that acts as a fortifying agent in medications and supplements. It's added to enhance the nutritional value of the product.

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

The official label also statesLanolin, Light Liquid Paraffin, Vitamin A, Vitamin D

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: 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.

🔁 Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Vitamin A D 93 g/100g 00404-0168-50	Henry	144 packets	—	—	FDA listed	—
AmeriDerm Vitamin A D 93 g/100g 52410-8037-02	Shield	100 g	—	—	FDA listed	—
Vitamins A and D Without Lanolin 93 g/100g 67777-0006-10	Dynarex	144 packets	—	—	FDA listed	—
Vitamin A D 93 g/100gthis 67777-0215-08	Dynarex	144 packets	—	—	FDA listed	—
Vitamin A D .93 g/g 68786-0213-01	Sion	144 packets	—	—	FDA listed	—
Gerigentle-Vitamins A and D .93 g/g 69771-0105-32	Geri-Gentle	5 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

🏛️

2022

On the market since

Mar 2022

📍

2026

Currently FDA-listed

4 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 Vitamin A D (this brand).

Top reported reactions

Pyrexia72

Rash68

Pneumonia61

Diarrhoea58

Nausea48

Febrile Neutropenia42

Anaemia41

Age at onset

Neonate5

Infant4

Child13

Adolescent6

Adult89

Elderly111

Reporter sex

Male · 56%

Female · 44%

Unknown · 0%

Serious outcomes

Hospitalization617

Death189

Life-threatening120

Disabling26

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
67777-0215-01	5 g in 1 PACKET (67777-215-01)	2013-10-01	Inactivated by FDA
67777-0215-08 You're viewing this	864 BOX in 1 CASE (67777-215-08) / 144 PACKET in 1 BOX (67777-215-07) / 5 g in 1 PACKET	2022-03-28	Active

Pack size FAQ

What quantity is in NDC 67777-0215-08?

NDC 67777-0215-08 is listed by the FDA — 864 box in 1 case / 144 packet in 1 box / 5 g in 1 packet.

What NDC number is used to bill for this package of Vitamin A D PETROLATUM 93 g/100g Ointment?

Bill NDC 67777-0215-08 — the 11-digit billing format is 67777021508. 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 67777-215-08, 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: 67777-0215-08, written without dashes as 67777021508. 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 67777-0215-08, the first segment (67777) is the labeler code FDA assigned to Dynarex Corporation; the middle segment (0215) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) 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 Dynarex 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 5 g (67777-0215-01). 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?

Dynarex 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose

🎯 Indications and Usage 51 words ▾

Use(s) • Helps treat chafed skin associated with diaper rash • Helps seal out wetness • Temporarily protects minor • Cuts • Scrapes • Burns • Temporarily helps protext and relieve chapped and cracked skin and lips • Helps prevent and protect from the drying effects of wind and cold weather

⏱️ Dosage and Administration 47 words ▾

Directions • Apply as needed • 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, and especially at bedtime or anytime when exposure to wet diapers may be prolonged.

⚠️ Warnings 81 words ▾

Warnings For External Use Only When using this product • Do not get into eyes Stop use and ask a doctor if • The condition persists or gets worse • Symptoms last more than 7 days or clear up and occur again in a few days Do not use on • Deep or 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

🧪 Active Ingredient 7 words ▾

Active Ingredient White Petrolatum, USP, 93% w/w

🧪 Inactive Ingredients 10 words ▾

Inactive Ingredients Lanolin, Light Liquid Paraffin, Vitamin A, Vitamin D

🎯 Purpose 3 words ▾

Purpose Skin Protectant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All Petrolatum NDCsSame ingredient 🏭 All Dynarex labeler NDCsLabeler code 67777 📖 Read the Petrolatum drug informationUses, warnings & side effects

💊 Related drugs in this class

Other drugs that share this product’s specific therapeutic class — Emollients.

Colloidal Oatmeal 00299-4128-00 Mineral Oil 00395-1673-28 Lanolin 53329-0042-44 Glycerin 67777-0233-02 Mineral Oil/Petrolatum,White 70942-0200-03

Where does this data come from?

Other drugs sharing this product’s First Databank therapeutic class (HIC3). Each links to that NDC’s page in our directory.