Label: LINDO HAND SANITIZER 59.2ML WITH CHERRY BLOSSOM GHA-211 01- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 54860-163-01 - 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 April 18, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- drug facts
- Warning
- Inactive ingredients
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Directions
Wet hands thoroughly with product and rub until dry without wiping
For children under 6,use only under adult supervision.
Not recommended for infants.
When using this product
Keep out of eyes,in case of contact with eyes,flush thoroughly with water
Do not inhale or ingest
Avoid contact with broken skin
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LINDO HAND SANITIZER 59.2ML WITH CHERRY BLOSSOM GHA-211 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54860-163 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 PRUNUS SPECIOSA FLOWER (UNII: A78OOO9299) 0.15 mL in 100 mL ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS) 0.1 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 CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.3 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:54860-163-01 59.2 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/18/2020 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(54860-163)