Label: CLEARSYNERGY- salicylic acid liquid
- NDC Code(s): 71617-100-10
- Packager: SRL ENTERPRISES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 8, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
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 acen medication at
the same time. If irritation occurs,
only use one topical acne medication
at a time. Limit use to face and neck.
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions:
Clean the skin thoroughly before
applying e product.
•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 to 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 INGREDIENT
- STORAGE AND HANDLING
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEARSYNERGY
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71617-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.25 g in 50 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:71617-100-10 1 in 1 BOX 09/07/2017 1 50 mL in 1 BOTTLE, PUMP; 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 09/07/2017 Labeler - SRL ENTERPRISES LLC (080452552) Establishment Name Address ID/FEI Business Operations Firm Name FDA Establishment Identifier DUNS Business Operations Address Expiration Date A.I.G. TECHNOLOGIES, INC. 086365223 manufacture(71617-100)