Label: SKINCEUTICALS BLEMISH PLUS AGE DEFENSE ACNE TREATMENT- salicylic acid lotion
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NDC Code(s):
49967-097-01,
49967-097-02,
49967-097-03,
49967-097-04, view more49967-097-05, 49967-097-06, 49967-097-07, 49967-097-08
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this 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 or 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
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SKINCEUTICALS BLEMISH PLUS AGE DEFENSE ACNE TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-097 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) METHYLPROPANEDIOL (UNII: N8F53B3R4R) GLYCOLIC ACID (UNII: 0WT12SX38S) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG) HYDROXYETHYLPIPERAZINE ETHANE SULFONIC ACID (UNII: RWW266YE9I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYQUATERNIUM-69 (350000 MW) (UNII: 7ZNS52Y987) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-097-01 1 in 1 CARTON 08/01/2005 08/01/2005 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-097-02 1 in 1 CARTON 08/01/2005 08/01/2005 2 55 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-097-03 1 in 1 CARTON 08/01/2005 08/01/2005 3 15 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:49967-097-04 6 in 1 CARTON 08/01/2005 08/01/2005 4 4 mL in 1 TUBE; Type 0: Not a Combination Product 5 NDC:49967-097-05 1 in 1 CARTON 08/01/2005 5 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 6 NDC:49967-097-06 1 in 1 CARTON 08/01/2005 6 55 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 7 NDC:49967-097-07 1 in 1 CARTON 08/01/2005 08/01/2005 7 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 8 NDC:49967-097-08 6 in 1 CARTON 08/01/2005 8 4 mL in 1 VIAL; 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 08/01/2005 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations Cosmetic Essence, LLC 032565959 manufacture(49967-097) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 pack(49967-097) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products, Inc. 624244349 manufacture(49967-097)