FDA.reportPublic FDA data

Pharmacys Prescription Petroleum Jelly

Manufacturer
American Consumer Products Corp
Effective date
2021-02-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:37:49

Label at a glance#

ProductPharmacys Prescription Petroleum Jelly
Active ingredientPETROLATUM
Label structure10 sections

Dosage and administration

Directions: Apply liberally as needed.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

White Petrolatum USP 100%

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive Ingredient • Fragrance

Purpose

OTC - PURPOSE SECTION

Purpose

Skin Protectant

Use

INDICATIONS & USAGE SECTION

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.

Warnings

WARNINGS SECTION

Warnings: For external use only • Do not apply over deep puncture wounds, infections, or lacerations.

OTC - ASK DOCTOR SECTION

If redness or swelling develops, consult a physician promptly.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Apply liberally as needed.

Other Information

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY:

American Consumer

Products Corp.

Vernon, CA 90058

Made in India

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacys Prescription Petroleum JellyPharmacys Prescription Petroleum Jelly

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204754petrolatum 100 % Topical JellyPSN3
204754petrolatum 1 MG/MG Topical OintmentSCD3
204754petrolatum 100 % Topical JellySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-040-062023-01-30C16284748780-1f386c64a-1bac-0266-e053-dadaa90a7c1aPharmacys Prescription Petroleum Jelly

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-040-06Pharmacys Prescription Petroleum Jelly170 g in 1 JARGEL1703

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-040PHARMACYS PRESCRIPTION PETROLEUM JELLY (PETROLATUM) GEL [AMERICAN CONSUMER PRODUCTS CORP]3Legacy NDC, 1 package rows20210206_b9819d7b-5c6b-8b8d-e053-2995a90a3af1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-04072197-040-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ba8ce181-b440-13ca-e053-2a95a90a22ebb9819d7b-5c6b-8b8d-e053-2995a90a3af12021-02-04WarningsExact identifier
spl id: ba8ce181-b440-13ca-e053-2a95a90a22eb
spl set id: b9819d7b-5c6b-8b8d-e053-2995a90a3af1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.