PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL- salicylic acid liquid

Pharmacys Prescription 8 OZ Acne Control by

Drug Labeling and Warnings

Pharmacys Prescription 8 OZ Acne Control by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active ingredient: Salicylic Acid 0.5%

Purpose

Purpose: Acne treatment

Uses: for the treatment of acne.

Warnings

Warnings: For external use only.

Flammable, keep away from open flame.

Keep out of reach of children

Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center immediately.

Inactive Ingredients

Water (aqua), Alcohol (24.5%), Propylene Glycol, Glycerin, PEG-32, Algae Extract, DMDM Hydantoin, Dimethicone Propyl PG-Betaine, Sodium Citrate, Aloe Barbadensis Leaf Extract, Benzophenone-4, Denatonium Benzoate, Fragrance, FD&C Yellow No..5.

Directions

Directions: Wash face as you normally would and pat dry with a clean towel. Apply a small amount to cotton ball or pad and applyu using a dabbing motion. Take care to avoid rubbing in eyes. Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy. Apply a light moisturizer after using astringent.

INSTRUCTIONS FOR USE

When using this product

- avoid contact with eyes. If contact occurs, immediately flush with water.

- using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used, unless directed by a doctor.

Indications & Usage

If bothersome drying or peeling occurs, reduce application.

Pharmacys Prescription 8 OZ Acne Control

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SULISOBENZONE (UNII: 1W6L629B4K)
PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-015-08	236.58 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/16/2019

Labeler - American Consumer Products Corp (081101181)