ANTISEPTIQUE PLUS- alcohol gel

Antiseptique Plus by

Drug Labeling and Warnings

Antiseptique Plus by is a Otc medication manufactured, distributed, or labeled by Hubot Healthcare LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl Alcohol 62.5% w/w

Purposes

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

• For external use only
• Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

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

• Apply product onto hands, spread thoroughly and rub dry

Other Information

• For additional information, see Safety Data Sheets (SDS)
• For emergency medical information in USA and Canada, call 1-888-255-3924
• For emergency medical information worldwide, call 1-813-248-0573

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)

INGREDIENTS AND APPEARANCE

ANTISEPTIQUE PLUS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72138-470
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72138-470-06	177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/13/2020
2	NDC: 72138-470-16	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/13/2020
3	NDC: 72138-470-32	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	03/13/2020

Labeler - Hubot Healthcare LLC (081084880)