Hand-Aid by ABC Compounding Co., Inc. HAND-AID- alcohol gel

Hand-Aid by

Drug Labeling and Warnings

Hand-Aid by is a Otc medication manufactured, distributed, or labeled by 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, triethanolamine, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis, dmdm hydantoin

Hand-Aid 6605 Drug Facts and Label

Hand-Aid 6605 Label

INGREDIENTS AND APPEARANCE

HAND-AID 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62257-122
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)
DMDM HYDANTOIN (UNII: BYR0546TOW)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62257-122-17	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2018
2	NDC: 62257-122-24	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2018
3	NDC: 62257-122-01	1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	11/12/2018
4	NDC: 62257-122-28	149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2018
5	NDC: 62257-122-14	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2018
6	NDC: 62257-122-13	800 mL in 1 BAG; Type 0: Not a Combination Product	11/12/2018
7	NDC: 62257-122-47	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/17/2020
8	NDC: 62257-122-17	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
9	NDC: 62257-122-55	208200 mL in 1 DRUM; Type 0: Not a Combination Product	03/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/12/2018

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

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

Establishment
Name	Address	ID/FEI	Business Operations
ABC Compounding Co., Inc.		003284353	manufacture(62257-122)