Label: CLEAR ACNE SPOT TREATMENT- acne spot treatment liquid
- NDC Code(s): 50718-0032-1
- Packager: Kamedis
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Drug Facts
When using this product
- avoid unnecessary sun exposure and use sunscreen
- avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water
- 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 at a time should be used, unless otherwise 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 1 to 3 times daily
- because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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
- for children under 10 years of age and under, consult your physician
Inactive Ingredients
acrylates/C10-30 alkyl acrylate crosspolymer, alcohol, amur cork tree (Phellodendron amurense) bark extract, baikal skullcap (Scutellaria baicalensis) root extract, benzyl alcohol, capryloyl glycine, Chinese rhubarb (Rheum palmatum) root extract, chlorphenesin, chrysanthemum (Chrysanthemum indicum) flower extract, cinnamon (Cinnamomum zeylanicum) bark extract, common purslane (Portulaca oleracea) extract, fragrance, glycerin, great burnet (Sanguisorba officinalis) root extract, hexylene glycol, Norway spruce (Picea abis) extract, propanediol, sarcosine, SD Alcohol 40-C, sodium phytate, tromethamine, water, xanthan gum
- SPL UNCLASSIFIED SECTION
- Carton label
-
INGREDIENTS AND APPEARANCE
CLEAR ACNE SPOT TREATMENT
acne spot treatment liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50718-0032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 28.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8) ALCOHOL (UNII: 3K9958V90M) PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) BENZYL ALCOHOL (UNII: LKG8494WBH) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) CHLORPHENESIN (UNII: I670DAL4SZ) CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L) PURSLANE (UNII: M6S840WXG5) GLYCERIN (UNII: PDC6A3C0OX) RHEUM PALMATUM ROOT (UNII: G025DAL7CE) SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PICEA ABIES WOOD (UNII: 72GZ8K8996) PROPANEDIOL (UNII: 5965N8W85T) SARCOSINE (UNII: Z711V88R5F) HEXASODIUM PHYTATE (UNII: ZBX50UG81V) TROMETHAMINE (UNII: 023C2WHX2V) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) CINNAMON BARK OIL (UNII: XE54U569EC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50718-0032-1 1 in 1 CARTON 01/01/2018 1 22 mL in 1 BOTTLE; 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 01/01/2018 Labeler - Kamedis (080311300) Establishment Name Address ID/FEI Business Operations Biogenesis Inc. 069117328 manufacture(50718-0032)