Label: AUQUEST ARMPIT REFRESHING ANTIPERSPIRANT SPRAY.- armpit refreshing antiperspirant spray spray
- NDC Code(s): 84186-010-01
- Packager: Guangzhou Bonnieco Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 1, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
- Other information
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Inactive ingredients
AQUA, PROPANEDIOL, ETHYLHEXYL PALMITATE, ZINC PHENOLSULFONATE, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, PORTULACA OLERACEA EXTRACT, PEG-100 STEARATE, ALLANTOIN, TOCOPHEROL, DIMETHICONE, CETEARYL ALCOHOL, ALUMINA, GLYCERYL STEARATE, PHENOXYETHANOL, HYDROXYETHYLCELLULOSE, ETHYLHEXYLGLYCERIN, PEG-20 STEARATE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AUQUEST ARMPIT REFRESHING ANTIPERSPIRANT SPRAY.
armpit refreshing antiperspirant spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84186-010 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 6 g in 100 mL Inactive Ingredients Ingredient Name Strength CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALUMINUM OXIDE (UNII: LMI26O6933) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TOCOPHEROL (UNII: R0ZB2556P8) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALLANTOIN (UNII: 344S277G0Z) WATER (UNII: 059QF0KO0R) ETHYLHEXYL PALMITATE (UNII: 2865993309) DIMETHICONE (UNII: 92RU3N3Y1O) PROPANEDIOL (UNII: 5965N8W85T) PURSLANE (UNII: M6S840WXG5) POLYOXYL 100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ZINC PHENOLSULFONATE (UNII: 4O71YT5YB5) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-20 STEARATE (UNII: NBX892EA57) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84186-010-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 04/02/2024 Labeler - Guangzhou Bonnieco Cosmetics Co., Ltd (412244189) Establishment Name Address ID/FEI Business Operations Guangzhou Bonnieco Cosmetics Co., Ltd 412244189 manufacture(84186-010) , label(84186-010)