Label: AIMERSIE HAND SANTIZER 500ML 01- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 54860-232-01 - Packager: Shenzhen Lantern Science Co.,Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 February 27, 2021
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INGREDIENTS AND APPEARANCE
AIMERSIE HAND SANTIZER 500ML 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54860-232 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) 0.15 mL in 100 mL WATER (UNII: 059QF0KO0R) 23.85 mL in 100 mL AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.09 mL in 100 mL CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.000008 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS) 0.1 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 mL in 100 mL Product Characteristics Color white (transparant) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54860-232-01 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/26/2020 Labeler - Shenzhen Lantern Science Co.,Ltd (421222423) Registrant - LANTERN HEALTH&BEAUTY LAB INC. (086860340) Establishment Name Address ID/FEI Business Operations Shenzhen Lantern Science Co., Ltd. 421222423 manufacture(54860-232)