Pharmacys Prescription Petroleum Jelly

Manufacturer: American Consumer Products Corp
Effective date: 2021-02-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:37:53

Label at a glance#

ProductPharmacys Prescription Petroleum Jelly

Active ingredientPETROLATUM

Label structure10 sections

Dosage and administration

Directions: Apply liberally to clean, dry diaper area.

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

USE: Helps treat and prevent diaper rash and seal out wetness.

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 to clean, dry diaper area.

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 Jelly

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
204754	petrolatum 100 % Topical Jelly	PSN	2
204754	petrolatum 1 MG/MG Topical Ointment	SCD	2
204754	petrolatum 100 % Topical Jelly	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72197-041-06	2023-01-30	C162847	48780-1	f386c649-cb19-0266-e053-dadaa90a7c1a	Pharmacys Prescription Petroleum Jelly Baby Fresh

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72197-041-06	Pharmacys Prescription Petroleum Jelly	170 g in 1 JAR	GEL	170		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72197-041	PHARMACYS PRESCRIPTION PETROLEUM JELLY (PETROLATUM) GEL [AMERICAN CONSUMER PRODUCTS CORP]	2	Legacy NDC, 1 package rows	20210207_b984a212-783f-8bc5-e053-2995a90a589c.zip

Products#

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

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

Pharmacys Prescription Petroleum Jelly
Petrolatum
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72197-041	72197-041-06

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
Name	UNII	Kind
PETROLATUM	4T6H12BN9U	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ba8cb716-a0c3-3910-e053-2995a90a2760			b984a212-783f-8bc5-e053-2995a90a589c	2021-02-04	Warnings	Exact identifier spl id: ba8cb716-a0c3-3910-e053-2995a90a2760 spl set id: b984a212-783f-8bc5-e053-2995a90a589c

Reported adverse events (FAERS/openFDA)#

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