AD PREVENT Original 15.5 g/100g; 53.4 g/100g Ointment
by WellSpring Pharmaceutical Corporation · 1 TUBE in 1 BOX (65197-401-01) / 113 g in 1 TUBE
NDC 65197-0401-01
🏷️ FDA NDC (as labeled)
65197-401-01
billing pads the product segment with a zero
This package
Contains113 g in 1 tube
Pack sizes4 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
65197-401-01
Product NDC
65197-401
11-digit billing NDC
65197040101
NCPDP billing unit
GM — per gram (weight)
RxCUI
664981
UNII
7EV65EAW6H, 4T6H12BN9U
Application #
M016
SPL Set ID
cf73246e-81c1-42e9-a107-dc6c99cf7d01
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2023-10-02
Route
TOPICAL
Dosage form
OINTMENT
Substance
LANOLIN; PETROLATUM
GCN Seq No
064809
GCN
16754
HICL code
036092
Ingredient (HICL)
Vits A And D/White Pet/Lanolin
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
A AND D OINTMENT
FDB brand name
A And D
Legend status
O — Over-the-counter (OTC) drug or device
Why two NDCs?
The FDA registers this code as 65197-401-01 — 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 → 65197-0401-01. 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
LabelerWellSpring Pharmaceutical Corporation
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code65197
First marketedOct 2023
Product typeHuman Otc Drug
Portfolio30 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.
🩺 Clinical
Label name A AND D OINTMENT Ingredient Vits A And D/White Pet/Lanolin
🧪 What is this product?
AD Prevent Original is a topical ointment containing lanolin and petrolatum, both emollient ingredients commonly used to soften and moisturize the skin. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for this category of skin protectant products rather than through an individual drug application. The combination of these ingredients is typically used to help soothe and protect dry or irritated skin areas.
Patient education
Supplement & herbal interactions
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.
💬 Questions about AD PREVENT Original?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
orange
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 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 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 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 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.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescod liver oil (contains vitamin A & vitamin D), fragrance, light mineral oil, microcrystalline wax, paraffin
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
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 |
|---|---|---|---|---|---|---|
| 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/g 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/100gthis 65197-0401-01 | WellSpring | 1 tube | — | — | 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
🏛️
2023
On the market since
Oct 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 65197-0401-00 | 454 g in 1 JAR (65197-401-00) | 2023-11-01 | Active |
| 65197-0401-01 You're viewing this | 1 TUBE in 1 BOX (65197-401-01) / 113 g in 1 TUBE | 2023-10-02 | Active |
| 65197-0401-12 | 1 TUBE in 1 BOX (65197-401-12) / 42.5 g in 1 TUBE | 2023-10-02 | Active |
| 65197-0401-99 | 567 g in 1 CARTON (65197-401-99) | 2025-07-01 | Active |
Pack size FAQ
What quantity is in NDC 65197-0401-01?
NDC 65197-0401-01 is listed by the FDA — 1 tube in 1 box / 113 g in 1 tube.
What NDC number is used to bill for this package of AD PREVENT Original 15.5 g/100g; 53.4 g/100g Ointment?
Bill NDC 65197-0401-01 — the 11-digit billing format is 65197040101. 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 65197-401-01, 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: 65197-0401-01, written without dashes as 65197040101. 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 65197-0401-01, the first segment (65197) is the labeler code FDA assigned to WellSpring Pharmaceutical Corporation; the middle segment (0401) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 WellSpring Pharmaceutical 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 3 other package presentations of this same product, including 1 tube (65197-0401-12), 454 g (65197-0401-00), 567 g (65197-0401-99). 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?
WellSpring Pharmaceutical 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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses helps treat and prevent diaper rash temporarily protects minor: cuts scrapes burns temporarily protects and helps relieve chapped or cracked skin and lips protects chafed skin due to diaper rash and helps seal out wetness
⏱️ Dosage and Administration ▾
Directions for skin protectant use: apply as needed for diaper rash use: 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 ▾
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 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.
📦 Storage and Handling ▾
Other information store between 20° to 25°C (68° to 77°F)
🧪 Active Ingredient ▾
Active Ingredients Lanolin 15.5% Petrolatum 53.4%
🧪 Inactive Ingredients ▾
Inactive ingredients cod liver oil (contains vitamin A & vitamin D), fragrance, light mineral oil, microcrystalline wax, paraffin
🎯 Purpose ▾
Purpose Diaper rash ointment Skin protectant
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.