Vaseline

Manufacturer: Conopco Inc. d/b/a Unilever | Alberto-Culver USA Inc.
Effective date: 2012-10-02
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:33:12

Label at a glance#

ProductVaseline Lip Therapy Advanced Formula

Active ingredientpetrolatum

Label structure9 sections

Contacts and useful links#

PhoneLabel contact1-800-457-7084

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
WHITE PETROLATUM, USP (100%)

OTC - PURPOSE SECTION

Purpose:
Skin Protectant

INDICATIONS & USAGE SECTION

Uses
▪ temporarily protects and helps relieve chapped or cracked skin and lips
▪ helps protect from the drying effects of wind and cold weather

WARNINGS SECTION

Warnings:
For External Use Only

OTC - WHEN USING SECTION

When using this product do not get into eyes

OTC - ASK DOCTOR SECTION

See a doctor if condition lasts more than 7 days

OTC - DO NOT USE SECTION

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.

DOSAGE & ADMINISTRATION SECTION

Directions apply as needed

INACTIVE INGREDIENT SECTION

Inactive Ingredient Flavor

OTC - QUESTIONS SECTION

Questions? Call 1-800-457-7084

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VLT 0.35 oz. PDPVaseline Lip Therapy Advanced 0.35 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VLT blister cardVaseline Lip Therapy Advanced 0.35 oz blister card

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
204754	petrolatum 100 % Topical Jelly	PSN	3
210871	Vaseline 100 % Topical Ointment	PSN	3
210871	petrolatum 1 MG/MG Topical Ointment [Vaseline]	SBD	3
204754	petrolatum 1 MG/MG Topical Ointment	SCD	3
204754	petrolatum 100 % Topical Jelly	SY	3
210871	Vaseline 1 MG/MG Topical Ointment	SY	3
210871	Vaseline 100 % Topical Ointment	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-0053-2	2020-01-31	C162847	48780-1	9d75b9d0-5b54-f424-e053-dadaa90a57ce	Vaseline Lip Therapy Advanced Formula

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-0053-1	VaselineLip Therapy Advanced Formula	10 g in 1 TUBE	OINTMENT	10		3
64942-0053-2	VaselineLip Therapy Advanced Formula	1 in 1 BLISTER PACK	OINTMENT	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-0053	VASELINE LIP THERAPY ADVANCED FORMULA (PETROLATUM) OINTMENT [CONOPCO INC. D/B/A UNILEVER]	3	Legacy NDC, 2 package rows	20121005_c4e87f3a-5e3b-4c9b-a1cd-21e9b3b625e3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
petrolatum	ACTIVE INGREDIENT	4T6H12BN9U	3
petrolatum	ACTIVE MOIETY	4T6H12BN9U	3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Vaseline Lip Therapy Advanced Formula
Petrolatum

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-0053	64942-0053-1, 64942-0053-2

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
Name	UNII	Kind
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
c22f300e-1305-4642-8472-087d5c67fc21			c4e87f3a-5e3b-4c9b-a1cd-21e9b3b625e3	2012-10-02	Warnings	Exact identifier spl id: c22f300e-1305-4642-8472-087d5c67fc21 spl set id: c4e87f3a-5e3b-4c9b-a1cd-21e9b3b625e3

Reported adverse events (FAERS/openFDA)#

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