Label: ANTISEPTIC HAND SANITIZER MINT SCENT- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 72762-004-15, 72762-004-16 - Packager: Two's Company, 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 June 18, 2021
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
For external use only
Flammable: Keep away from heat and flame
When using this product
• do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water
• do not apply to irritated or broken skin.Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72 hours. -
Directions
• lift tab and spray a small amount into the palms of your hands and forearms.
• wet the hands thoroughly with product, rub hands together and allow to dry without wiping • no rinsing required.
• children under 6 years of age should be supervised when using this product • not recommended for infants.
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
ANTISEPTIC HAND SANITIZER MINT SCENT
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72762-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 mL in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72762-004-16 1 in 1 BLISTER PACK 09/01/2018 1 NDC:72762-004-15 15 mL in 1 BOTTLE, SPRAY; 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 part333E 09/01/2018 Labeler - Two's Company, Inc. (056307960)
