Label: ALMAY CLEAR COMPLEXION CONCEALER- salicylic acid liquid
- NDC Code(s): 0311-0725-30
- Packager: ALMAY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 June 1, 2021
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- ACTIVE INGREDIENT
-
OTHER INGREDIENTS
AQUA/WATER/EAU, CYCLOPENTASILOXANE, GLYCERIN, KAOLIN, DIMETHICONE, BORON NITRIDE, TRIBEHENIN, PEG/
PPG-18/18 DIMETHICONE, TRIMETHYLSILOXYSILICATE, METHYL METHACRYLATE CROSSPOLYMER, CETYL PEG/PPG-10/1 DIMETHICONE, PEG-10 DIMETHICONE, HYDROLYZED VEGETABLE PROTEIN, POLYETHYLENE, ALOE BARBADENSIS LEAF JUICE, MARIS SAL/SEA SALT/SEL MARIN, SILICA, 1,2-HEXANEDIOL, ALPHA-GLUCAN OLIGOSACCHARIDE, CAPRYLYL GLYCOL, LACTOBACILLUS, MALTODEXTRIN, PERLITE, POLYISOBUTENE, POLYMNIA SONCHIFOLIA ROOT JUICE, TETRASODIUM EDTA, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE, TRISILOXANE, PHENOXYETHANOL. MAY
CONTAIN: [+/- : IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), TITANIUM DIOXIDE (CI 77891), ZINC OXIDE (CI 77947).] - USE
- WARNING
-
DIRECTIONS
• Clean skin thoroughly before applying this product
• Cover 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
• Sensitivity test for a new user apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions above - WARNINGS
- PURPOSE
- ART
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INGREDIENTS AND APPEARANCE
ALMAY CLEAR COMPLEXION CONCEALER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0311-0725 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 mg in 2 mL Inactive Ingredients Ingredient Name Strength 1,2-HEXANEDIOL (UNII: TR046Y3K1G) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) WATER (UNII: 059QF0KO0R) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) BORON NITRIDE (UNII: 2U4T60A6YD) FERROSOFERRIC OXIDE (UNII: XM0M87F357) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) PHENOXYETHANOL (UNII: HIE492ZZ3T) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) SEA SALT (UNII: 87GE52P74G) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PERLITE (UNII: 0SG101ZGK9) TRIBEHENIN (UNII: 8OC9U7TQZ0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TRIMETHYLSILOXYSILICATE (M/Q 0.66) (UNII: 5041RX63GN) ZINC OXIDE (UNII: SOI2LOH54Z) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) SMALLANTHUS SONCHIFOLIUS LEAF (UNII: AX57ELY8YM) TRISILOXANE (UNII: 9G1ZW13R0G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) EDETATE SODIUM (UNII: MP1J8420LU) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) KAOLIN (UNII: 24H4NWX5CO) LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHICONE (UNII: 92RU3N3Y1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0311-0725-30 9 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/05/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 03/05/2021 Labeler - ALMAY (064988652) Establishment Name Address ID/FEI Business Operations REVLON 809725570 manufacture(0311-0725)
