Label: MAYBELLINE DREAM PURE BB BEAUTY BALM- salicylic acid lotion
- NDC Code(s): 49967-957-01
- 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.
-
Directions
- clean the skin thoroughly before apply 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
-
Inactive ingredients
water, dimethicone, isododecane, glycerin, diisostearyl malate, kaolin, disteardimonium hectorite, polydimethylsiloxyethyl dimethicone, sodium chloride, phenoxyethanol, dimethicone/polyglycerin-3 crosspolymer, PEG-10 dimethicone, sodium hydroxide, sodium dehydroacetate, chlorphenesin, disodium stearoyl glutamate, acrylates copolymer, tocopherol, ascorbyl palmitate, aluminum hydroxide, PEG-9, dipropylene glycol glutamate, propylene carbonate, aluminum hydroxide; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MAYBELLINE DREAM PURE BB BEAUTY BALM
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-957 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic acid 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-957-01 30 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2014 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 624244349 manufacture(49967-957)