FDA.reportPublic FDA data

Vaseline

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2026-03-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:50:35

Label at a glance#

ProductVaseline
Active ingredientPETROLATUM
Label structure9 sections

Indications and uses

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

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

WHITE PETROLATUM, USP (100%)

Purpose

OTC - PURPOSE SECTION

skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily protects minor

  • cuts
  • scrapes
  • burns

temporarily protects and helps relieve chapped or cracked skin and lips

helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only
When using this product do not get into eyes
See a doctor if condition last more than 7 days
Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

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

apply as needed

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

Questions?

OTC - QUESTIONS SECTION

Call 1-800-457-7084

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vaseline Healing JellyVaseline Healing Jelly

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204754petrolatum 100 % Topical JellyPSN4
210871Vaseline 100 % Topical OintmentPSN4
210871petrolatum 1 MG/MG Topical Ointment [Vaseline]SBD4
204754petrolatum 1 MG/MG Topical OintmentSCD4
204754petrolatum 100 % Topical JellySY4
210871Vaseline 1 MG/MG Topical OintmentSY4
210871Vaseline 100 % Topical OintmentSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1874-12026-01-29C16284748780-149896155-ad1c-586f-e063-e6dba90add90Vaseline Healing Jelly
64942-1874-22026-01-29C16284748780-149896155-ad1c-586f-e063-e6dba90add90Vaseline Healing Jelly
64942-1874-32026-01-29C16284748780-149896155-ad1c-586f-e063-e6dba90add90Vaseline Healing Jelly
64942-1874-42026-01-29C16284748780-149896155-ad1c-586f-e063-e6dba90add90Vaseline Healing Jelly
64942-1874-52026-01-29C16284748780-149896155-ad1c-586f-e063-e6dba90add90Vaseline Healing Jelly

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1874-1Vaseline49 g in 1 JARJELLY494
64942-1874-2Vaseline71 g in 1 TUBEJELLY714
64942-1874-3Vaseline106 g in 1 JARJELLY1064
64942-1874-4Vaseline212 g in 1 JARJELLY2124
64942-1874-5Vaseline368 g in 1 JARJELLY3684
64942-1874-6Vaseline49 g in 1 TUBEJELLY494
64942-1874-7Vaseline193 g in 1 TUBEJELLY1934

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-187464942-1874-1, 64942-1874-2, 64942-1874-3, 64942-1874-4, 64942-1874-5, 64942-1874-6, 64942-1874-7

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
NameUNIIKind
WATER059QF0KO0RIACT
PETROLATUM4T6H12BN9UACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VaselineHEALING JELLYConopco Inc. d/b/a Unileverbd4418b7-c6aa-5e71-e053-2995a90a4cc42026-03-16WarningsExact identifier
ndc (package): 64942-1874-3
ndc (package): 64942-1874-4
ndc (package): 64942-1874-2
ndc (package): 64942-1874-7
ndc (package): 64942-1874-5
ndc (package): 64942-1874-6
ndc (package): 64942-1874-1
ndc (product): 64942-1874
ndc11 (package): 64942187407
ndc11 (package): 64942187404
ndc11 (package): 64942187405
ndc11 (package): 64942187403
ndc11 (package): 64942187401
ndc11 (package): 64942187406
ndc11 (package): 64942187402
spl id: 4d263aff-9ee2-4980-e063-6394a90a95c0
spl set id: bd4418b7-c6aa-5e71-e053-2995a90a4cc4

Reported adverse events (FAERS/openFDA)#

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