ANTISEPTIQUE 70- alcohol gel

Antiseptique 70 by

Drug Labeling and Warnings

Antiseptique 70 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 70% v/v

Purposes

Antiseptic

Uses

to help reduce bacteria on 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 | On children less than 2 years of age | On open skin wounds

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

|Place enough product on hands to cover all surfaces. Rub hands together until dry | Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

| Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F) | For additional information, see Safety Data Sheets (SDS)

Inactive Ingredients

water (aqua), propylene glycol, dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl Acrylate Crosspolymer, aminomethylpropanediol, tocopherol acetate, aloe barbadensis leaf juice

Questions?

sales@tri-pac.us

PRINCIPAL DISPLAY PANEL - 946 ML Bottle Label

ANTISEPTIQUE+70
gel sanitizer

antiseptic | rinse-free | 70% alcohol

FOR HANDS
dye free, fragrance free

FOR HEALTHCARE PROFESSIONALS ONLY

32 FL. OZ. (946 ML)

INGREDIENTS AND APPEARANCE

ANTISEPTIQUE 70 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72138-460
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)
Propylene Glycol (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
DIMETHICONE PEG-8 ISOSTEARATE (UNII: JGV7463UFN)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
Tocopherol (UNII: R0ZB2556P8)
Aloe Vera Leaf (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72138-460-06	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/25/2020
2	NDC: 72138-460-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/25/2020
3	NDC: 72138-460-16	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/25/2020
4	NDC: 72138-460-32	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	06/25/2020

Labeler - Hubot Healthcare LLC (081084880)