Label: NITOUCH ALCOHOL HAND SANITIZER- ethyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 80437-002-01 - Packager: Kasa Trading, Llc
- 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 September 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
- PURPOSE
- Uses
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Warnings
• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product: Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Do not inhale
or ingest.
• Do not use in children less than 2 months of age.
• Stop use and ask a doctor if irritation or a rash develops.
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
NITOUCH ALCOHOL HAND SANITIZER
ethyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80437-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80437-002-01 250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/08/2020 Labeler - Kasa Trading, Llc (080477332)