PETROLEUM JELLY- white petrolatum jelly

Petroleum Jelly by

Drug Labeling and Warnings

Petroleum Jelly by is a Otc medication manufactured, distributed, or labeled by Aldermed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

White petrolatum USP 100%

Purpose

Skin protectant

Uses

temporarily protects minor

• cuts
• scrapes
• burns
• temporarily protects and chafed, chapped or cracked skin
• helps prevent against the drying effects of wind and cold weather

Warnings

For external use only

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

In swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

apply as needed

Other information

• store at 15-30 C (59-86F)

Inactive ingredients

none

Questions or comments?

Call 1-833-605-84-74 9am-5 pm EST M-F

Distributror

Distributor:
ALDERMED INC.
7901 4TH ST N STE 300 ST PETERSBURG, FL 33702
www.aldermed.us MADE IN INDIA MH/DRUGS/25-KD/739

Package Label

INGREDIENTS AND APPEARANCE

PETROLEUM JELLY 
white petrolatum jelly

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WHITE PETROLATUM (UNII: B6E5W8RQJ4) (WHITE PETROLATUM - UNII:B6E5W8RQJ4)	WHITE PETROLATUM	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-009-02	56.6 g in 1 TUBE; Type 0: Not a Combination Product	12/01/2025
2	NDC: 87236-009-13	368 g in 1 JAR; Type 0: Not a Combination Product	12/01/2025
3	NDC: 87236-009-15	425 g in 1 JAR; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/01/2025

Labeler - Aldermed Inc. (144887712)

Registrant - Aldermed Inc. (144887712)