ANTISEPTIQUE 70- 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+70

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)

PRINCIPAL DISPLAY PANEL - 946 ML Bottle Label
ANTISEPTIQUE 70 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72138-460
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72138-460-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/25/2020
2NDC:72138-460-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/25/2020
3NDC:72138-460-16473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
4NDC:72138-460-32946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E06/25/2020
Labeler - Hubot Healthcare LLC (081084880)

Revised: 6/2020
Document Id: d715d706-add6-471f-bbfa-42db129affd5
Set id: e94b59b1-7f18-4688-a4e3-4cc338af4f45
Version: 1
Effective Time: 20200629
 
Hubot Healthcare LLC