Label: TOMRICK CARE HAND SANITIZER 59ML HXE0005 01- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 54860-258-01 - Packager: Shenzhen Lantern Scicence 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 May 9, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Features
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Warning
For external use only-hands
Avoid eyes. In case of eye contact,flush with water.
Flammable,Keep away from heat and flame.
Discontinue if skin becomes irritated and ask a doctor.
keep out of reach of children,in case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately.
- Inactive ingredients
- Directions
- Purpose
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TOMRICK CARE HAND SANITIZER 59ML HXE0005 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54860-258 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 .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 mL in 100 mL ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS) 0.01 mL in 100 mL ALOE (UNII: V5VD430YW9) 0.15 mL in 100 mL CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.3 mL in 100 mL AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.09 mL in 100 mL WATER (UNII: 059QF0KO0R) 23.85 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 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:54860-258-01 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/09/2020 Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423) Registrant - Lantern Beauty America,INC. (117371139) Establishment Name Address ID/FEI Business Operations Shenzhen Lantern Science Co.,Ltd. 421222423 manufacture(54860-258)
