ACNE SHAVE MOISTURIZER- salicylic acid cream

Acne Shave Moisturizer by

Drug Labeling and Warnings

Acne Shave Moisturizer by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

Salicylic acid 0.5%.................................Acne medication

PURPOSE

Use

for the management of acne

WARNINGS

Warnings

For external use only

WHEN USING

When using this product

• skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE

Directions

• cleanse the skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three times daily
• excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times if needed or as directed by a doctor
• if dryness or peeling occurs, reduce application to once a day or every other day

INACTIVE INGREDIENT

Inactive ingredients

Water, Dicaprylyl Carbonate, Pentylene Glycol, Cetearyl Alcohol, Dimethicone, Dicetyl Phosphate, Ceteth-10 Phosphate, Aluminum Starch Octenylsuccinate, Melia Azardirachta Seed Oil, Allantoin, Xanthan Gum, Steareth-20, Hydroxyacetophenone, Methyl Gluceth-20, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, 1,2-Hexanediol, Methyl Lactate, Sodium Hydroxide, Disodium EDTA

DOSAGE & ADMINISTRATION

Distributed by:

17211 Valley View

Cerritos, CA 90703 USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNE SHAVE MOISTURIZER 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T)
ALLANTOIN (UNII: 344S277G0Z)
STEARETH-20 (UNII: L0Q8IK9E08)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
METHYL LACTATE, DL- (UNII: H10S91526X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-112-03	98 mL in 1 TUBE; Type 0: Not a Combination Product	07/25/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	07/25/2017

Labeler - United Exchange Corp. (840130579)