Petrolatum Jelly

Manufacturer: CRYSTAL CURAM
Effective date: 2019-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:59:21

Label at a glance#

ProductPetrolatum Jelly

Active ingredientPETROLATUM

Label structure11 sections

Indications and uses

temporarily protects minor cuts, scrapes, burns and sunburn temporarily protects and helps relieve chapped or cracked skin helps protect from the drying effects of wind and cold weather helps treat and prevent diaper rash helps seal out wetness

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

White Petrolatum (99.5% w/w)

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily protects minor cuts, scrapes, burns and sunburn
temporarily protects and helps relieve chapped or cracked skin
helps protect from the drying effects of wind and cold weather
helps treat and prevent diaper rash
helps seal out wetness

Warnings:

WARNINGS SECTION

FOR EXTERNAL USE ONLY

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms last for more than 7 days or clean up and occur again in a few days

Do not use on

OTC - DO NOT USE SECTION

deep or puncture wounds
animal bites
serious burns

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display & Drug Fact

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2122757	petrolatum 99.5 % Topical Jelly	PSN	1
2122757	petrolatum 0.995 MG/MG Topical Gel	SCD	1
2122757	petrolatum 99.5 % Topical Gel	SY	1
2122757	white petrolatum 99.5 % Topical Jelly	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72886-6662-0	2021-01-29	C162847	48780-1	ba0f9c33-402a-a910-e053-dadaa90a0b85	CRYSTAL COCOA BUTTER
72886-6662-3	2021-01-29	C162847	48780-1	ba0f9c33-402a-a910-e053-dadaa90a0b85	CRYSTAL COCOA BUTTER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72886-6662-0	Petrolatum Jelly	170 g in 1 JAR	JELLY	170		1
72886-6662-3	Petrolatum Jelly	369 g in 1 JAR	JELLY	369		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72886-6662	PETROLATUM JELLY (PETROLATUM) JELLY [CRYSTAL CURAM]	1	Legacy NDC, 2 package rows	20190430_8624bb24-fd28-28ee-e053-2a91aa0ad823.zip

Products#

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

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

Petrolatum Jelly
Petrolatum
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72886-6662	72886-6662-3, 72886-6662-0

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
WATER	059QF0KO0R	IACT
PETROLATUM	4T6H12BN9U	ACTIB

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
8624bb24-fd27-28ee-e053-2a91aa0ad823			8624bb24-fd28-28ee-e053-2a91aa0ad823	2019-04-09	Warnings	Exact identifier spl id: 8624bb24-fd27-28ee-e053-2a91aa0ad823 spl set id: 8624bb24-fd28-28ee-e053-2a91aa0ad823

Reported adverse events (FAERS/openFDA)#

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