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Gerigentle-Vitamins A and D Petrolatum .93 g/g Ointment — NDC 69771-0105-33 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Gerigentle-Vitamins A and D Petrolatum .93 g/g Ointment — NDC 69771-105-33 (Billing 69771-0105-33)

by Geri-Gentle Corporation · 12 TUBE in 1 CARTON / 113 g in 1 TUBE

This is a package of Gerigentle-Vitamins A and D Petrolatum .93 g/g Ointment from Geri-Gentle Corporation, marketed since Jan 2015 and currently FDA-listed.

NDC 69771-0105-33
🏷️ FDA NDC (as labeled) 69771-105-33 billing pads the product segment with a zero
This package
Contains113 g in 1 tube Pack sizes2 compare ↓
Product page 69771-0105-32 Also comes in: 5 g 69771-105-32
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69771-105-33
Product NDC 69771-105
11-digit billing NDC 69771010533
RxCUI 1440181
UNII 4T6H12BN9U
UPC 0648289160116
Application # M016
SPL Set ID c36c74f7-975b-4e4c-99e3-e6921d782c71
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-01-15
Route TOPICAL
Dosage form OINTMENT
Substance PETROLATUM
Quick answers
  • RxCUI (RxNorm): 1440181
Why two NDCs? The FDA registers this code as 69771-105-33 — 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 → 69771-0105-33. 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?

Gerigentle-Vitamins A and D is a topical ointment containing petrolatum as its active ingredient. Petrolatum is commonly used as an occlusive moisturizer and skin protectant in over-the-counter products. It functions to help trap moisture in the skin and create a protective barrier. This is an OTC monograph drug, meaning it is marketed under FDA's established guidelines for this category of product.

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.

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: 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
69771-0105-32 69771-105-32 Main listing 5 g in 1 PACKET 2015-01-15 — Active
69771-0105-33 You're viewing this 12 TUBE in 1 CARTON / 113 g in 1 TUBE 2015-01-15 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 12 tube in 1 carton / 113 g in 1 tube.
What NDC number is used to bill for this package of Gerigentle-Vitamins A and D Petrolatum .93 g/g 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
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/100g 67777-0215-01 Dynarex 5 g — — Discontinued —
Vitamin A D .93 g/g 68786-0213-01 Sion 144 packets — — FDA listed —
Gerigentle-Vitamins A and D .93 g/gthis 69771-0105-33 Geri-Gentle 12 tubes — — 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
Jan 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 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 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 L4SQI4K87S
    A synthetic yellow dye used as a colorant in medicines. It gives tablets, capsules, or liquids their yellow color to help identify the drug and make it visually distinct.
  • UNII 81G40H8B0T
    Vitamin A is a fat-soluble nutrient that acts as a colorant and antioxidant in medications. It prevents oxidation of other ingredients and may add nutritional value to the formulation.
  • 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.

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

The official label also statesLanolin, Lavender Fragrance, Light Liquid Paraffin, Paraffin, Vitamin A, Vitamin D, CI 12740

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

LabelerGeri-Gentle Corporation
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code69771
First marketedJan 2015
Product typeHuman Otc Drug
Portfolio22 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 ⏱️ Dosage and Administration ⚠️ Warnings 📦 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 69 words ▾

Uses Helps treat and prevent diaper rash Helps seal out wetness Temporarily protects minor cuts scrapes burns Temporarily helps protect and relieve chapped and cracked skin or lips Helps prevent and protect from the drying effects of wind and cold weather Helps prevent and protect chafed skin or minor skin irritations associated with diaper rash With each diaper change, especially at bedtime when exposure to wetness may be prolonged

⏱️ Dosage and Administration 23 words ▾

Directions for use with Diaper Rash change wet and soiled diaper promptly cleanse the diaper area and allow to dry apply as needed

⚠️ Warnings 67 words ▾

Warnings For external use only When using this product Do not get into eyes Stop Use and consult a doctor if condition worsens symptoms last more than 7 days symptoms clear up and reoccur in a few days Do not use on deep puncture wounds animal bites serious burns Keep out of reach of children! If swallowed, get medical help or contact a Poison Control Center immediately

📦 Storage and Handling 11 words ▾

Other information store at 15°-30°C (59°-86°F) avoid excessive heat and humidity

🧪 Active Ingredient 6 words ▾

Active ingredient White Petrolatum USP (93%w/w)

🧪 Inactive Ingredients 15 words ▾

Inactive Ingredients Lanolin, Lavender Fragrance, Light Liquid Paraffin, Paraffin, Vitamin A, Vitamin D, CI 12740

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Do Not Use 11 words ▾

Do not use on deep 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 24 words ▾

Stop Use and consult a doctor if condition worsens symptoms last more than 7 days symptoms clear up and reoccur in 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 9 words ▾

PRINCIPAL DISPLAY PANEL Principal Display and Drug Fact Panel

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 Geri-Gentle 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 (69771-0105-32). 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?
Geri-Gentle 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.
← 69771-0091-38 · Geri-Gentle 69771-0106-34 · Geri-Gentle →
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.