FDA.reportPublic FDA data

Cruex Petroleum Jelly

Manufacturer
MKJ BRANDS LLC
Effective date
2026-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-18 05:10:18

Label at a glance#

ProductCruex Petroleum Jelly
Active ingredientPETROLATUM
Label structure7 sections

Indications and uses

temporarily protects ■ minor cuts, scrapes, burns ■ and help relieve chapped or cracked skin and lips ■ from the drying effects of wind and cold weather

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

White Petrolatum USP 30%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily protects ■ minor cuts, scrapes,
burns ■ and help relieve chapped or cracked
skin and lips ■ from the drying effects of wind and
cold weather

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and consult a doctor

OTC - STOP USE SECTION

if the condition lasts more than 7 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. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf extract, frafrance, tocopheryl acetate, water, glycerin, gelyceryl stearate, PEG-100 Stearate, stearic acid, sodium hydroxide, Lanolin alcohol, Fragrance, Acrylates 10-30 alkyl acrylate crosspolymer, pheonxyethanol, triethylene glycol, dospdoium EDTA

Petrolatum Jelly

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

vasel (1)vasel (1)

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77782-00477782-004-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
LANOLIN ALCOHOL884C3FA9HEIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
SODIUM HYDROXIDE55X04QC32IIACT
STEARIC ACID4ELV7Z65APIACT
AQUA059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CETEARETH-20YRC528SWUYIACT
PETROLATUM4T6H12BN9UACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
EDETATE DISODIUM7FLD91C86KIACT
PEG-100 MONOSTEARATEYD01N1999RIACT
TRIETHYLENE GLYCOL3P5SU53360IACT
GLYCERYL STEARATE230OU9XXE4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-12-10full-release2026-06-01 01:21:39

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
Cruex Petroleum JellyWHITE PETROLATUMMKJ BRANDS LLC459a90b8-7d52-ef70-e063-6394a90ac1d02026-07-14WarningsExact identifier
ndc (package): 77782-004-13
ndc (product): 77782-004
ndc11 (package): 77782000413
spl id: 5697710a-a3d3-230c-e063-6294a90a447c
spl set id: 459a90b8-7d52-ef70-e063-6394a90ac1d0

Reported adverse events (FAERS/openFDA)#

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