Label: HAND SANITIZER- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79091-009-01 - Packager: HAAN BRAND SL
- 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 August 28, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Uses
- Active Ingredient
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Warnings
- For external use only- hands
- When using this product keep out o f eyes. In case of contact, flush throughly with water.
- Do Not Inhale or ingest.
- Avoid contact with broken skin
- Keep out of reach of children. In case of incidental ingestion seek professional assistance or contact a Poison Control Center inmediately.
- Stop use and ask Doctor: if skin irritation develops.
- Flammable: Keep away from heat and flame.
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive Ingredients
- Questions?
- Uses
- Hand Sanitizer Gel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79091-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER 934 (UNII: Z135WT9208) METHYL GLUCETH-10 (UNII: N0MWT4C7WH) WATER (UNII: 059QF0KO0R) LIMONENE, (+)- (UNII: GFD7C86Q1W) ALOE VERA LEAF (UNII: ZY81Z83H0X) LINALOOL, (+)- (UNII: F4VNO44C09) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) TROMETHAMINE (UNII: 023C2WHX2V) BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79091-009-01 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/18/2020 Labeler - HAAN BRAND SL (468886727) Registrant - HAAN BRAND SL (468886727) Establishment Name Address ID/FEI Business Operations Laboratorios Magrina SL 460356033 manufacture(79091-009) Establishment Name Address ID/FEI Business Operations HAAN BRAND SL 468886727 label(79091-009)