Recens by Certus Medical, Inc. / ABC Compounding Co., Inc. RECENS- alcohol gel

Recens by

Drug Labeling and Warnings

Recens by is a Otc medication manufactured, distributed, or labeled by Certus Medical, Inc., ABC Compounding Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Box OTC-Active Ingredient Section

Ethyl Alcohol 62%

Drug Facts Box OTC-Purpose Section

Antiseptic

Drug Facts Box OTC-Indications & Usage Section

for hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

FLAMMABLE, keep away from fire and flames

For external use only

Drug Facts Box OTC-When Using Section

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box OTC-Stop Use Section

irritation and redness develop

Drug Facts Box OTC-Keep Out of Reach of Children Section

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

Drug Facts Box OTC-Dosage & Administration Section

wet hands thoroughly with product and allow to dry without wiping

Drug Facts Box OTC-Inactive Ingredient Section

water, diisopropylamine, carbomer, propylene glycol, DMDM hydantoin, tocopheryl acetate, aloe barbadensis

Recens Gel 6966 1000ml

Recens Gel 1000ml 

INGREDIENTS AND APPEARANCE

RECENS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75990-605
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75990-605-24	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/16/2019
2	NDC: 75990-605-01	1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	10/16/2019
3	NDC: 75990-605-03	350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	10/16/2019
4	NDC: 75990-605-05	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/16/2019
5	NDC: 75990-605-07	700 mL in 1 BAG; Type 0: Not a Combination Product	10/16/2019
6	NDC: 75990-605-10	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	10/16/2019
7	NDC: 75990-605-11	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/16/2019
8	NDC: 75990-605-12	1000 mL in 1 BAG; Type 0: Not a Combination Product	10/16/2019
9	NDC: 75990-605-13	800 mL in 1 BAG; Type 0: Not a Combination Product	10/16/2019
10	NDC: 75990-605-28	149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/16/2019
11	NDC: 75990-605-27	800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	10/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/16/2019

Labeler - Certus Medical, Inc. (966433653)

Registrant - ABC Compounding Co., Inc. (003284353)

Establishment
Name	Address	ID/FEI	Business Operations
ABC Compounding Co., Inc.		003284353	manufacture(75990-605)