PETROLEUM JELLY- petrolatum jelly

Petroleum Jelly by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Petrolatum

keep out of reach of children

Keep out of reach of children

Purpose

Gentell petroleum Jelly temporarily protects minor cuts, scraped, and burns. It temporarily protects and helps relieve chapped, chafered, or cracked skin and lips, and helps protect from the drying effects of wind and col weather.

Indications & useage

Gentell Petroleum Jelly temporarily protects minor cuts, scrapes, and burns. It temporarily protects and helps relieve chapped, chafed, or cracked skin and lips, and helps protect from the drying effects of wind and cold weather.

Dosage & Administration

Apply as needed

Warnings Section

For external use only

When using this product,do not get into eyes

Stop use and ask a doctor if condition worsens or if symptoms last more than seven days or clear up and occur again within a few days

Do not use on deep or puncture wounds, animal bites or serious burns

Keep out of reach of children

If swallowed, get medical help or contact a Poison control Center right away

Inactive Ingredients

There are no inactive ingredients

Petroleum Jelly

Gentell

Petroleum Jelly

Skin Protectant

GEN-23750 13oz.(369g)

Gentell 2701 Bartram Road, Bristol, PA 19007 www.gentell.com

INGREDIENTS AND APPEARANCE

PETROLEUM JELLY 
petrolatum jelly

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61554-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61554-600-01	5 g in 1 POUCH; Type 0: Not a Combination Product	11/13/2014
2	NDC: 61554-600-02	113.4 g in 1 TUBE; Type 0: Not a Combination Product	11/13/2014
3	NDC: 61554-600-03	368.5 g in 1 JAR; Type 0: Not a Combination Product	11/13/2014
4	NDC: 61554-600-04	453.6 g in 1 JAR; Type 0: Not a Combination Product	11/13/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/13/2014

Labeler - Gentell, Inc. (170967876)

Establishment
Name	Address	ID/FEI	Business Operations
Gentell, Inc.		170967876	manufacture(61554-600)