VASELINE INTENSIVE CARE ALOE FRESH PROTECTING BODY LOTION- spf 15 lotion

Vaseline Intensive Care by

Drug Labeling and Warnings

Vaseline Intensive Care by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a Unilever, Unilever Supply Chain Co. d/b/a Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

WARNING:  FOR EXTERNAL USE ONLY.  AVOID EYE CONTACT.  RINSE WITH WATER TO REMOVE.  IF RASH OR IRRITATION DEVELOPS, STOP USE AND ASK A DOCTOR.  KEEP AWAY FROM CHILDREN.  IF SWALLOWED, CONTACT A POISON CONTROL CENTER RIGHT AWAY.

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:  OCTINOXATE (7.5%)
OXYBENZONE (3.0%)  OCTISALATE (1.0%)

INACTIVE INGREDIENT

Water, Stearic Acid, Glycerin, Isopropyl
Palmitate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Euterpe
Oleracea (Acai) Fruit Extract, Camellia Sinensis (Green Tea)
Leaf Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopheryl
Acetate, Retinyl Palmitate, Dimethicone, Potassium Lactate,
Lactic Acid, Collagen Amino Acids, Glycine Soja (Soybean) Sterol,
Lecithin, Petrolatum, Helianthus Annuus (Sunflower) Seed Oil or
Glycine Soja (Soybean) Oil, Sodium PCA, Sodium Stearoyl-2-Lactylate,
Urea, Mineral Water, Glyceryl Stearate, Carbomer, Cetyl Alcohol,
Magnesium Aluminum Silicate, Fragrance, Potassium Hydroxide,
DMDM Hydantoin, Disodium EDTA, Methylparaben, Propylparaben,
Titanium Dioxide.

PRINCIPAL DISPLAY PANEL

PDP 20.3 oz front

PRINCIPAL DISPLAY PANEL

PDP 20.3 oz back

QUESTIONS

Questions section

INGREDIENTS AND APPEARANCE

VASELINE INTENSIVE CARE  ALOE FRESH PROTECTING BODY LOTION
spf 15 lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1048
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	7.5 mL  in 100 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	3.0 mL  in 100 mL
Octisalate (UNII: 4X49Y0596W) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Octisalate	1.0 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1048-1	600 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	12/23/2008

Labeler - Conopco Inc. d/b/a Unilever (001375088)

Establishment
Name	Address	ID/FEI	Business Operations
Unilever Supply Chain Co. d/b/a Unilever		043510056	manufacture