ANTACGEL- hand sanitizer gel with peppermint and lavender, 73% alcohol gel 
MEDIPHARCO PHARMACEUTICAL JOINT STOCK COMPANY

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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Alcohol 73%

Antiseptic

Hand sanitizer gel helps to sanitize hands, eliminate unpleasant odor and leave hands feeling soft and fresh.

For external use only. Flammable. Keep away from the heat or flame.

* in children less than 2 months of age
* on open skin wounds

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

if irritation or rash occurs. These may be signs of a serious condition.

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

* Apply a proper amount of gel to one hand. Thoroughly rub your hand together until dry.
* Supervise children under 6 years of age when using this product to avoid swallowing.
* Store below 86ºF (30ºC)
* May discolor certain fabrics or surfaces

Blue (C.I. 42090), Carbomer, Isopropyl myristate, Lavender oil, Peppermint oil, Purified water, Red (C.I. 45430), Triethanolamine.

Apply a proper amount of gel to one hand.

Hand Sanitizer Gel with Peppermint and LavenderHand Sanitizer Gel with Peppermint and Lavender

ANTACGEL 
hand sanitizer gel with peppermint and lavender, 73% alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79633-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL73 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
LAVENDER OIL (UNII: ZBP1YXW0H8)  
TROLAMINE (UNII: 9O3K93S3TK)  
ERYTHROSINE SODIUM ANHYDROUS (UNII: 8TL7LH93FM)  
WATER (UNII: 059QF0KO0R)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79633-202-25217 g in 1 BOTTLE; Type 0: Not a Combination Product07/22/2020
2NDC:79633-202-45434 g in 1 BOTTLE; Type 0: Not a Combination Product07/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/22/2020
Labeler - MEDIPHARCO PHARMACEUTICAL JOINT STOCK COMPANY (555273697)
Establishment
NameAddressID/FEIBusiness Operations
MEDIPHARCO PHARMACEUTICAL JOINT STOCK COMPANY555273697manufacture(79633-202)

Revised: 7/2020
Document Id: ab01e72f-d073-0549-e053-2995a90ad7d8
Set id: ab01e72f-d072-0549-e053-2995a90ad7d8
Version: 1
Effective Time: 20200722
 
MEDIPHARCO PHARMACEUTICAL JOINT STOCK COMPANY