![NU SKIN CLEAR ACTION (SALICYLIC ACID) GEL [NSE PRODUCTS, INC.]](https://medic.hrt.org//dailymed/images/be125d02-b74a-49bd-90e6-2eac6f513923/nuskin-01.jpg)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
- For external use only. Using other topical acne medication at the same time or immediately following the 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.
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Cleanse the skin thoroughly before applying medication.
- Cover the entire affected area with a thin layer once daily.
- If bothersome dryness or peeling occurs, reduce application to every other day.
Inactive ingredients
Water (Aqua), Butylene Gylcol, Methyl Gluceth-20, Ethoxydiglycol, Polyacrylamide, Cyclodextrin/Retinol, Thioctic Acid,1 Tocopheryl Acetate, Camellia Sinensis Leaf Extract, Phytosphingosine, Glycyrrhiza Glabra (Licorice) Root Extract, Glycerin, Laureth-7, C13-14 Isoparaffin, BHT, Sodium Hydroxide, Tetrasodium EDTA, Fragrance (Parfum), Chlorphenesin, Methylparaben, Propylparaben.
- 1
- Alpha Lipoic Acid.
- PRINCIPAL DISPLAY PANEL - 30 ml Carton
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INGREDIENTS AND APPEARANCE
NU SKIN CLEAR ACTION ACNE MEDICATION NIGHT TREATMENT
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-0390 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 g in 1000 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Methyl Gluceth-20 (UNII: J3QD0LD11P) Diethylene Glycol Monoethyl Ether (UNII: A1A1I8X02B) Alpha Lipoic Acid (UNII: 73Y7P0K73Y) Green Tea Leaf (UNII: W2ZU1RY8B0) Glycyrrhiza Glabra (UNII: 2788Z9758H) Glycerin (UNII: PDC6A3C0OX) Laureth-7 (UNII: Z95S6G8201) C13-14 Isoparaffin (UNII: E4F12ROE70) Butylated Hydroxytoluene (UNII: 1P9D0Z171K) Sodium Hydroxide (UNII: 55X04QC32I) Edetate Sodium (UNII: MP1J8420LU) Chlorphenesin (UNII: I670DAL4SZ) Methylparaben (UNII: A2I8C7HI9T) Propylparaben (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-0390-1 1 in 1 CARTON 1 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 09/01/2010 Labeler - NSE Products, Inc. (966817975)
