SALICYLIC FACE AND BODY WASH- salicylic acid soap liquid

Salicylic Face and Body Wash by

Drug Labeling and Warnings

Salicylic Face and Body Wash by is a Otc medication manufactured, distributed, or labeled by CosMedical Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Acne treatment

WARNINGS

For external use only

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INACTIVE INGREDIENT

Water,

Sodium Lauroyl
Methyl Isethionate

Sodium Chloride

Glycerin
Cocamide MIPA

Decyl Glucoside

Cocos Nucifera (Coconut) Oil

Cyamopsis Tetragonoloba (Guar) Gum

Aloe Barbadensis Leaf Juice

Salix Nigra (Willow) Bark Extract

Glyceryl Caprylate

CitricAcid

Sodium Hydroxide

Glyceryl Undecylenate

ACTIVE INGREDIENT

Salicylic Acid 2.0%

INDICATIONS & USAGE

Acne Treatment

DOSAGE & ADMINISTRATION

Topical

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SALICYLIC FACE AND BODY WASH 
salicylic acid soap liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70060-1503
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.02 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAUROYL METHYL ISETHIONATE (UNII: II6VCD3S6R)
GLYCERIN (UNII: PDC6A3C0OX)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCONUT OIL (UNII: Q9L0O73W7L)
GUAR GUM (UNII: E89I1637KE)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SALIX NIGRA BARK (UNII: QU52J3A5B3)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70060-1503-1	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/04/2015
2	NDC: 70060-1503-2	360 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/04/2015
3	NDC: 70060-1503-3	1.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/04/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/04/2015

Labeler - CosMedical Technologies (803898329)

Registrant - CosMedical Technologies (803898329)

Establishment
Name	Address	ID/FEI	Business Operations
CosMedical Technologies		803898329	relabel(70060-1503)