CLEARSYNERGY- salicylic acid cloth

ClearSynergy by

Drug Labeling and Warnings

ClearSynergy by is a Otc medication manufactured, distributed, or labeled by SRL Enterprises, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne Treatment

Uses

For the treatment of acne.

Warnings

For external use only.

When using this product:Avoid contact with eyes and mouth. If contact occurs, rinse thoroughly with water. 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 acne medication at a time. Limit use to face and neck.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Cover the entire affected area with a thin layer one to three times daily.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive ingredients

Water, Sodium PCA, Ammonium Lauryl Sulfate, Succinic Acid, Phosphoric Acid.

STORAGE AND HANDLING

• Store in a cool, dry place
• Do not freeze

Questions or comments?support@srlclear.com

ProductLabel

INGREDIENTS AND APPEARANCE

CLEARSYNERGY 
salicylic acid cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71617-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
SUCCINIC ACID (UNII: AB6MNQ6J6L)
PHOSPHORIC ACID (UNII: E4GA8884NN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71617-102-01	30 in 1 PACKAGE	05/31/2020
1		150 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/31/2020

Labeler - SRL Enterprises, LLC (080452552)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc.		161104729	manufacture(71617-102)