Aloe Vera Petrolatum Jelly

Manufacturer: Shield Line LLC
Effective date: 2025-08-15
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:10:46

Label at a glance#

ProductAloe Vera Petrolatum 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 (99.35% 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

Aloe vera extract, Vitamin E , Fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display and Drug Fact Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2639233	petrolatum 99.4 % Topical Ointment	PSN	3
2639233	petrolatum 0.994 MG/MG Topical Ointment	SCD	3
2639233	petrolatum 99.35 % Topical Ointment	SY	3
2639233	petrolatum 99.4 % Topical Ointment	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52410-1030-3	2025-08-15	C162847	48780-1	2cef2736-7fa0-d83d-e063-dadaa90ab31f	Aloe Vera Petroleum Jelly
52410-1030-5	2025-08-15	C162847	48780-1	2cef2736-7fa0-d83d-e063-dadaa90ab31f	Aloe Vera Petroleum Jelly
52410-1030-3	2025-01-30	C162847	48780-1	2cef2736-7fa0-d83d-e063-dadaa90ab31f	Aloe Vera Petroleum Jelly
52410-1030-5	2025-01-30	C162847	48780-1	2cef2736-7fa0-d83d-e063-dadaa90ab31f	Aloe Vera Petroleum Jelly

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52410-1030-3	Aloe Vera Petrolatum Jelly	226 g in 1 JAR	JELLY	226		3
52410-1030-5	Aloe Vera Petrolatum Jelly	368 g in 1 JAR	JELLY	368		3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Aloe Vera Petrolatum Jelly
Petrolatum
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52410-1030	52410-1030-5, 52410-1030-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
PETROLATUM	4T6H12BN9U	ACTIB
.ALPHA.-TOCOPHEROL	H4N855PNZ1	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
Aloe Vera Petrolatum Jelly	PETROLATUM	Shield Line LLC	fdf3b90e-a434-49b2-e053-6394a90ab175	2025-08-15	Warnings	Exact identifier ndc (package): 52410-1030-5 ndc (package): 52410-1030-3 ndc (product): 52410-1030 ndc11 (package): 52410103005 ndc11 (package): 52410103003 spl id: 3c6a536d-4c6b-595a-e063-6394a90a3f44 spl set id: fdf3b90e-a434-49b2-e053-6394a90ab175

Reported adverse events (FAERS/openFDA)#

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