Hand Prep Antiseptic Hand Sanitizer

Hand Prep Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

Hand Prep Antiseptic Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sanco Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND PREP ANTISEPTIC HAND SANITIZER- isopropyl alcohol gel 
Sanco Industries, Inc.

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.

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Hand Prep Antiseptic Hand Sanitizer

Drug Facts

Active ingredient

Isopropyl alcohol 72.2%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only
Flammable, keep away from fire or flame

Do not use

  • in the eyes
  • on open skin wounds

Stop use and ask a doctor if

  • Irritation and redness develop
  • Condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping

Other Information

  • Store between 59-104°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

Purified water, glycerin, methacrylic acid ethyl acrylate polymer, FD&C Blue No. 1

Questions or comments

(260)-426-6281

Package Labeling:

Label

HAND PREP ANTISEPTIC HAND SANITIZER 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80248-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.722 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80248-000-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/202009/09/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/23/202009/09/2022
Labeler - Sanco Industries, Inc. (617275354)

Revised: 7/2021
 

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