PETROLEUM JELLY- petrolatum jelly

Petroleum Jelly by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Petrolatum 100% ......................................... Skin Protectant

PURPOSE

Skin Protectant

WARNINGS

Warnings

For external use only When using this product do not get into eyes Stop use and ask a doctor if

condition worsens symptoms last more than 7 days or clear up and occur again within a few days. Do not
use on deep or puncture wounds animal bites serious burns. . Keep out of reach of children. If
swallowed, get medical help or contact a Poison Control Center right away.

ASK DOCTOR

Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days.

STORAGE AND HANDLING

Other Information .

Store between 68° F to 77° F (20° to 25°() and avoid direct sunlight.

INSTRUCTIONS FOR USE

Directions

Apply as needed

DOSAGE & ADMINISTRATION

apply as needed

INACTIVE INGREDIENT

No inactive ingredients. Not applicable

INDICATIONS & USAGE

Uses
Temporarily protects minor . cuts . scrapes . burns. Temporarily protects and helps relieve chapped, chafed or cracked skin and lips. Helps protect from the frying effect of wind and cold weather.

KEEP OUT OF REACH OF CHILDREN

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

Principal Display Panel

INGREDIENTS AND APPEARANCE

PETROLEUM JELLY 
petrolatum jelly

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64772-202
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: 64772-202-01	113 g in 1 TUBE; Type 0: Not a Combination Product	11/13/2014
2	NDC: 64772-202-02	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 - Derma Sciences Canada Inc. (200564891)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Sciences Canada Inc.		200564891	manufacture(64772-202) , label(64772-202)