Label: ATP HAND SANITIZER- ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73960-001-02 - Packager: East West Brands Inc.
- 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 21, 2020
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- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only: hands.
Flammable. Keep away from fire or flame.
When using this product ▪ Keep out of eyes, ears, or mouth. ▪ In case of eye contact, flush eyes thoroughly with water. ▪ Avoid contact with broken skin. ▪ Do not inhale or ingest.
Stop use and ask a doctor if ▪ redness or irritation develop and persist ▪ condition persists for more than 72 hours.
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
ATP HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73960-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TROLAMINE (UNII: 9O3K93S3TK) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73960-001-02 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/21/2020 Labeler - East West Brands Inc. (080642088)