ANTISEPTIQUE PLUS- alcohol gel 
Hubot Healthcare LLC

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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Antiseptique Plus

Drug Facts

Active ingredient

Ethyl Alcohol 62.5% w/w

Purposes

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

Do not use

  • In eyes

When using this product

  • If in eyes, rinse promptly and thoroughly with water
  • Discontinue use if irritation and redness develops

Stop use and ask a doctor if skin irritation or redness occurs or 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

Other Information

Inactive Ingredients

water (aqua), ethyl acrylate/ methacrylic acid/ steareth-20 methacrylate copolymer, aminomethylpropanediol, ppg-14 butyl ether, tocopherol acetate, aloe barbadensis leaf juice

Questions?

Call 1-855-CLEAN-55 (253-2655)

PRINCIPAL DISPLAY PANEL - 473 ML Bottle Label

ANTISEPTIQUE+
PLUS
gel sanitizer

antiseptic | rinse-free | 62.5% alcohol

FOR HANDS
dye free, fragrance free

16 FL. OZ. (473 ML)

PRINCIPAL DISPLAY PANEL - 473 ML Bottle Label
ANTISEPTIQUE PLUS 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72138-470
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
Tocopherol (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72138-470-06177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/13/2020
2NDC:72138-470-16473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/13/2020
3NDC:72138-470-32946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E03/13/2020
Labeler - Hubot Healthcare LLC (081084880)

Revised: 3/2020
Document Id: 71a4771b-e392-45f2-9ec3-fe427d97f1a8
Set id: 6dc7f218-363f-4bf4-ae0a-1155bbdc6f19
Version: 1
Effective Time: 20200318
 
Hubot Healthcare LLC