COCOA BUTTER PETROLEUM JELLY- petrolatum cream

COCOA BUTTER PETROLEUM jelly by

Drug Labeling and Warnings

COCOA BUTTER PETROLEUM jelly by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Drug Facts

Active ingredient:

Petrolatum 30%

​Purpose

Skin Protectant

​Uses

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

​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 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.

​Directions

apply as needed.

​Inactive ingredients:

water (aqua), mineral oil, glycerin, cetearyl alcohol, cetyl alcohol, stearyl alcohol, glyceryl stearate, fragrance, polysorbate 80, laureth-20, BHT, methylparaben, propylparaben, dimethicone, tocopherol.

SPL UNCLASSIFIED SECTION

New

Vitamin E

Moisturizing

with Cocoa Butter Extra Rich

​Compare to the active ingredient of Vaseline​® ​Petroleum Jelly Cream*

Tones, softens & smooths dry skin

Distributed by:
Universal Distribution Center
96 Distribution Boulevard Edison, NJ 08817
www.universaldc.com

Made in P.R.C

Packaging

INGREDIENTS AND APPEARANCE

COCOA BUTTER PETROLEUM JELLY 
petrolatum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	30 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
LAURETH-20 (UNII: 6SU0SC83AH)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-124-35	133 mL in 1 TUBE; Type 0: Not a Combination Product	07/27/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/27/2015

Labeler - Universal Distribution Center LLC (019180459)