Label: CLEAR CELL SALICYLIC CLARIFYING TONIC- salicylic acid and glycolic acid liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 62742-4043-1 - Packager: Allure Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 22, 2010
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
INDICATIONS & USAGE
INDICATIONS AND USAGE SECTION:
A salicylic/glycolic acid skin clarifying removes excess surface oil. A blend of anti-oxidants leaves skin fresh and shine-free.
Paraben Free
DIRECTIONS:
Saturate gauze and gently remove surface oils. Repeat if necessary for additional clarifying and toning.
INDICATIONS:
Acne and acne-prone skin
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
Deionized water (Aqua), Hamamelis virginiana (Witch Hazel) water, Glycerin, Mentha viridis (Spearmint) Oil, Camellia oleifera (Green Tea) leaf extract, Ammonium Hydroxide, Melaleuca alternifolia (Tea tree) leaf oil, Arnica montana flower extract, Chamomile reticutita flower (Chamomile) extract, Aesculus hippocastanum (Horse Chestnut) extract, Melia azadirachta (Neem) extract, Eucalyptus globulus (Eucalyptus) oil.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEAR CELL SALICYLIC CLARIFYING TONIC
salicylic acid and glycolic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4043 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 30 mg in 1 mL GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID 50 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4043-1 118 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 01/01/2010 Labeler - Allure Labs, Inc. (926831603)
