Label: LUSETA RINSE FREE HAND SANITIZER- hand sanitizer solution
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Contains inactivated NDC Code(s)
NDC Code(s): 74159-440-03, 74159-440-17, 74159-440-34 - Packager: Guangzhou Beaver Cosmetic 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 8, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
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When using this product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - Stop use
- Keep out of reach of children.
- Directions
- Other information
- Inactive Ingredients
- Drug Facts
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INGREDIENTS AND APPEARANCE
LUSETA RINSE FREE HAND SANITIZER
hand sanitizer solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74159-440 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 GLYCERIN (UNII: PDC6A3C0OX) CARBOMER 940 (UNII: 4Q93RCW27E) DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9) TROMETHAMINE (UNII: 023C2WHX2V) ALOE ANDONGENSIS LEAF (UNII: N1P4NU25EJ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GRAPE (UNII: 6X543N684K) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74159-440-34 1000 in 1 BOTTLE 04/30/2020 1 NDC:74159-440-17 500 in 1 BOTTLE 1 NDC:74159-440-03 75 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/30/2020 Labeler - Guangzhou Beaver Cosmetic Co., Ltd (420020595) Registrant - Guangzhou Beaver Cosmetic Co., Ltd (420020595) Establishment Name Address ID/FEI Business Operations Guangzhou Beaver Cosmetic Co., Ltd 420020595 manufacture(74159-440)