FDA.reportPublic FDA data

Petroleum Jelly

Manufacturer
Davion, Inc.
Effective date
2022-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:45:35

Label at a glance#

ProductPetroleum Jelly
Active ingredientPETROLATUM
Label structure6 sections

Indications and uses

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

Directions:

DOSAGE & ADMINISTRATION SECTION

apply as needed

Warnings:

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION


  • do not get into eyes.

See a doctor if

OTC - ASK DOCTOR SECTION

if condition worsens or 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.

Principal Label Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


NDC 42669-214-06

Perfect Purity

Pure Petroleum Jelly

GUARANTEED PURE 100% PURE

NET WT. 6 OZ. (170 g)



Label 1
Label 1


NDC 42669-214-13

Perfect Purity

Petroleum Jelly

Skin Protectant

For minor cuts, scrapes and burns

NET WT. 13 OZ. (369 g)



Label 2
Label 2




FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42669-214-062022-12-05C16284748780-19d75b9d0-f4ae-f424-e053-dadaa90a57ceDrug Facts
42669-214-132022-12-05C16284748780-19d75b9d0-f4ae-f424-e053-dadaa90a57ceDrug Facts
42669-214-062020-01-31C16284748780-19d75b9d0-f4ae-f424-e053-dadaa90a57ceDrug Facts
42669-214-132020-01-31C16284748780-19d75b9d0-f4ae-f424-e053-dadaa90a57ceDrug Facts

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42669-21442669-214-06, 42669-214-13

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
01e28e43-f763-69da-e063-6394a90afbe5dc064fa4-b61c-4099-a759-f37ea014f0872023-08-01WarningsExact identifier
spl set id: dc064fa4-b61c-4099-a759-f37ea014f087

Reported adverse events (FAERS/openFDA)#

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