Petrolatum Jelly

Manufacturer: ASTONEA LABS PRIVATE LIMITED
Effective date: 2023-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:53:15

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 drying effect of wind and cold weather helps treat and prevent diaper rash help seal out wetness

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

White Petrolatum (99.9% 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 drying effect of wind and cold weather
helps treat and prevent diaper rash
help seal out wetness

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

When using this product

OTC - WHEN USING SECTION

do not get into the 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 and Drug Fact PanelPrincipal Display and Drug Fact PanelPrincipal Display and Drug Fact Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1148414	petrolatum 99.9 % Topical Gel	PSN	1
1148414	petrolatum 0.999 MG/MG Topical Gel	SCD	1
1148414	petrolatum 99.9 % Topical Jelly	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77338-101-03	2025-01-30	C162847	48780-1	2cef2736-a65f-d83d-e063-dadaa90ab31f	ASTONEA 99.9%
77338-101-05	2025-01-30	C162847	48780-1	2cef2736-a65f-d83d-e063-dadaa90ab31f	ASTONEA 99.9%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77338-101-03	Petrolatum Jelly	226 g in 1 JAR	JELLY	226		1
77338-101-05	Petrolatum Jelly	368 g in 1 JAR	JELLY	368		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77338-101	PETROLATUM JELLY (PETROLATUM) JELLY [ASTONEA LABS PRIVATE LIMITED]	1	Legacy NDC, 2 package rows	20230113_f2160a9e-efca-dd8b-e053-2a95a90a98da.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
77338-101	77338-101-03, 77338-101-05

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
f216106d-2254-fc25-e053-2a95a90aeff8			f2160a9e-efca-dd8b-e053-2a95a90a98da	2023-01-12	Warnings	Exact identifier spl id: f216106d-2254-fc25-e053-2a95a90aeff8 spl set id: f2160a9e-efca-dd8b-e053-2a95a90a98da

Reported adverse events (FAERS/openFDA)#

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