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Advanced Healing Petrolatum 410 mg/g Ointment, 56 g — NDC 21130-0247-16 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Advanced Healing Petrolatum 410 mg/g Ointment, 56 g — NDC 21130-247-16 (Billing 21130-0247-16)

by Better Living Brands, LLC · 56 g in 1 TUBE

This is a package of 56 g of Advanced Healing Petrolatum 410 mg/g Ointment from Better Living Brands, LLC, no longer marketed (first marketed Jul 2015), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 21130-0247-16
🏷️ FDA NDC (as labeled) 21130-247-16 billing pads the product segment with a zero
This package
Contains56 g Pack sizes2 compare ↓
Main listing for product 21130-247 · Also comes in: 50 g 21130-247-17
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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

NDC database record

One package, one record: these facts belong to NDC 21130-247-16 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
21130 labeler · 247 product · 16 package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 2113024716 6
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 21130-247-16
Product NDC 21130-247
11-digit billing NDC 21130024716
RxCUI 725145
UNII 4T6H12BN9U
Application # M016
SPL Set ID ba50f2b2-aff8-42cd-8af0-369060a901fb
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2015-07-15
Route TOPICAL
Dosage form OINTMENT
Substance PETROLATUM
Quick answers
  • RxCUI (RxNorm): 725145
Why two NDCs? The FDA registers this code as 21130-247-16 — 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 → 21130-0247-16. 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?

Advanced Healing Petrolatum is a topical ointment containing petrolatum as its active ingredient. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for this category of skin protectants. Petrolatum is commonly used to help protect and soften skin by forming an occlusive barrier that reduces moisture loss. This type of product is typically applied to areas of dry, chapped, or irritated skin.

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: 50 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
21130-0247-17 21130-247-17 50 g in 1 TUBE 2015-07-15 — Active
21130-0247-16 You're viewing this Main listing 56 g in 1 TUBE 2015-07-15 — Discontinued by firm

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 56 g — 56 g in 1 tube.
How does this package differ from NDC 21130-0247-17?
Both are Advanced Healing Petrolatum 410 mg/g Ointment — the drug itself is identical. This page's package is the 56 g one, while NDC 21130-0247-17 is the 50 g package.
What NDC number is used to bill for this package of Advanced Healing Petrolatum 410 mg/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
Leader Baby Skin Protectant 41 g/100g 70000-0079-01 Cardinal 85 g $0.054 — Availability likely —
Walgreens Baby Healing 410 mg/g 00363-0079-50 Walgreens 50 g — — FDA listed —
Advanced Healing 410 mg/g 00363-9247-17 Walgreen 50 g — — FDA listed —
Aquaphor Original 41 g/100g 10356-0100-37 Beiersdorf 396 g — — FDA listed —
Aquaphor Healing 41 g/100g 10356-0101-02 Beiersdorf 7 g — — FDA listed —
Skin protectant 410 mg/g 11344-0247-17 Nice-Pak 50 g — — FDA listed —
Target Up and Up Healing Petrolatum Skin Protectant 410 mg/g 11673-0234-59 TARGET 396 g — — FDA listed —
Target Baby Healing 410 mg/g 11673-0729-85 Target 85 g — — FDA listed —
Advanced Healing 410 mg/g 11822-1247-04 Rite 396 g — — FDA listed —
Hydrating Healing 410 mg/g 13709-0353-01 Neilmed 1 tube — — FDA listed —
Advanced Healing 410 mg/gthis 21130-0247-16 Better 56 g — — Discontinued —
Healing 410 mg/g 36800-0247-41 Topco 396 g — — FDA listed —
Skin Protectant 410 mg/g 41190-0180-21 Wakefern 85 g — — FDA listed —
Healing 410 mg/g 41250-0059-16 Meijer, 56 g — — Discontinued —
Healing for Babies 410 mg/g 41250-0997-17 Meijer, 50 g — — FDA listed —
Advanced Healing 410 mg/g 49035-0875-17 Walmart 50 g — — FDA listed —
Advanced Healing 410 mg/g 55319-0952-17 Family 50 g — — FDA listed —
ProCure HydroShield 41 g/100g 55681-0045-04 Twin 106 g — — FDA listed —
Healing for Babies 410 mg/g 55910-0180-21 Old 85 g — — FDA listed —
Advanced Healing 410 mg/g 55910-0965-17 Old 50 g — — FDA listed —
Healing Cream 3oz 41 g/100g 57337-0166-01 Rejoice 85 g — — FDA listed —
Healing Cream15oz 41 g/100g 57337-0171-01 Rejoice 425 g — — FDA listed —
Advanced Healing 41 g/100g 57337-0193-01 Rejoice 57 g — — FDA listed —
Healing Cream 3oz 41 g/100g 58503-0201-01 China 85 g — — FDA listed —
Healing Cream 15oz 41 g/100g 58503-0206-01 China 425 g — — FDA listed —
Advanced Healing 410 mg/g 59779-0086-06 CVS 198 g — — FDA listed —
Hydrating Healing Skin Protectant 41 g/100g 59779-0853-03 CVS 85 g — — FDA listed —
Cvs 41 g/100g 63148-0178-14 Apollo 397 g — — FDA listed —
Advanced Healing 410 mg/g 64024-0247-17 Aldi, 50 g — — FDA listed —
AquaSoothe 41 g/100g 67777-0555-02 Dynarex 24 tubes — — FDA listed —
CR-5667753 Leader Daily Moisturizer 41 g/100g 70000-0059-01 Cardinal 1 tube — — FDA listed —
Petrolatum 410 mg/g 72288-0180-17 Amazon.com 50 g — — Discontinued —
Advanced Healing 410 mg/g 72288-0247-17 Amazon.com 50 g — — Discontinued —
Advanced Healing 410 mg/g 72476-0247-17 Retail 1 tube — — FDA listed —
Skin Protectant 410 mg/g 79903-0329-07 Walmart 198 g — — FDA listed —
Advanced Healing 410 mg/g 82442-0247-07 Target 198 g — — FDA listed —
Hydrating 41 g/100g 87236-0010-37 Aldermed 106 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
Jul 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 Q1LS2UJO3A
    Ceresin is a purified mineral wax derived from ozocerite. It functions as a binding agent, thickener, and coating material in medicines to help hold ingredients together and provide texture or protective coating.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 884C3FA9HE
    Lanolin alcohol is a waxy substance derived from sheep's wool. It functions as an emollient and emulsifier in medicines, helping blend oil and water-based ingredients while softening the product's texture.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.

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

The official label also statesmineral oil, ceresin, lanolin alcohol, panthenol, glycerin, bisabolol

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

LabelerBetter Living Brands, LLC
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code21130
First marketedJul 2015
Product typeHuman Otc Drug
Portfolio84 products on file

More NDCs from Better Living Brands, LLC labeler code 21130

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 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 32 words ▾

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

⏱️ Dosage and Administration 4 words ▾

Directions apply as needed

⚠️ Warnings 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 39 words ▾

ADVERSE REACTION DISTRIBUTED BY BETTER LIVING BRANDS, LLC P.O. BOX 99, PLEASANTON, CA 94566-0009 ‡1-888-723-3929 *This product is not manufactured or distributed by Beiersdorf Inc., distributor of Aquaphor Healing Ointment. PLASTIC TUBE how2recycle.info smartlabel Scan here for more information

🧪 Active Ingredient 4 words ▾

Active ingredient Petrolatum 41%

🧪 Inactive Ingredients 10 words ▾

inactive ingredients mineral oil, ceresin, lanolin alcohol, panthenol, glycerin, bisabolol

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 When Using This Product 9 words ▾

When using this product do not get into eyes

📄 Stop Use and Ask a Doctor If 26 words ▾

Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again with in 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 72 words ▾

principal display panel Signature Care Quality Guaranteed COMPARE TO Aquaphor Healing Ointment* ADVANCED Healing Ointment Skin Protectant For dry, cracked or irritated skin Fragrance-free Non-irritating Net Wt

1.75 OZ (50 g) image description

PRINCIPAL DISPLAY PANEL COMPARE TO Aquafor ® Healing Ointment* Signature SELECT ® ADVANCED HEALING OINTMENT SKIN PROTECTANT FOR DRY, CRACKED OR IRRITATED SKIN FRAGRANCE-FREE NON-IRRITATING LOVE IT OR IT'S ON US‡ NET WT

1.75 OZ (50 g) image description

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

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 Advanced Healing (this brand).

Top reported reactions

Rash45
Pneumonia31
Pruritus31
Cellulitis29
Dyspnoea24
Urinary Tract Infection24
Dizziness23

Reporter sex

435 reports

Serious outcomes

Hospitalization260
Life-threatening49
Disabling8
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 71 30
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 50 g (21130-0247-17). 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?
Better Living Brands, LLC 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.
← 21130-0243-26 · Safeway 21130-0248-75 · Better →
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.