CLEAR REFLECTION COMPLEXION ACNE TREATMENT SERUM- salicylic acid 2% gel

Clear Reflection Complexion Acne Treatment Serum by

Drug Labeling and Warnings

Clear Reflection Complexion Acne Treatment Serum by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

2 percent Salicylic Acid

WARNINGS

For external use only.

DO NOT USE

Do not use this medication if you have very sensitive skin or if you are sensitive to salicylic acid.

WHEN USING

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 medication at a time.

Avoid contact with the eyes

If contact occurs, rinse 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 right away.

DOSAGE & ADMINISTRATION

Directions

In the morning, after cleansing face, apply serum evenly and make sure all problem areas are treated. Mild tingling may occur. If bothersome dryness occurs, reduce application to once every other day.

INACTIVE INGREDIENT

Cyclopentasiloxane, Dimethiconol, Isopropyl Alcohol, Octyldodecanol, Helianthus Annuus (Sunflower) Seed Oil, Dimethicone, Dihydroeugenol, Isoeugenyl, Cinnamal, Ethyl Vanilla.

PURPOSE

Acne Treatment

INDICATIONS & USAGE

Recommended use is in the morning after cleansing and before applying any makeup.

QUESTIONS

Call Customer Service at 1 800 990 6552 or contact customerservice@dermamedics.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLEAR REFLECTION COMPLEXION ACNE TREATMENT SERUM 
salicylic acid 2% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-685
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1.04 g  in 52 mL

Inactive Ingredients
Ingredient Name	Strength
CINNAMALDEHYDE (UNII: SR60A3XG0F)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ISOEUGENYL ACETATE (UNII: 9DF21GI8W6)
ETHYL VANILLIN (UNII: YC9ST449YJ)
DIHYDROEUGENOL (UNII: A3XE712277)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
OCTYLDODECANOL (UNII: 461N1O614Y)
DIMETHICONOL (50000 CST) (UNII: R2285D73YT)
DIMETHICONE 12500 (UNII: D1R3R4B8M8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-685-02	52 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	10/30/2023

Labeler - Renu Laboratories, Inc. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories, Inc.		945739449	manufacture(76348-685)