GBG ALOEGEL- alcohol gel

GBG AloeGel by

Drug Labeling and Warnings

GBG AloeGel by is a Otc medication manufactured, distributed, or labeled by HealthLink, 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

Antimicrobial

Drug Facts Box OTC-Indications & Usage Section

to sanitize hands without requiring water or a rinse

Drug Facts Box OTC-Warnings Section

FLAMMABLE

For external use only

Drug Facts Box OTC-When Using Section

do not use near heat or open flame

do not use in or near eyes

discontinue use if irritation and redness develop

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

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Drug Facts Box OTC-Dosage & Administration Section

apply gel liberally to unsoiled hands and rub in thoroughly

allow to dry without wiping or rinsing

Drug Facts Box OTC-General Precautions Section

store at room temperature

Drug Facts Box OTC-Inactive Ingredient Section

Water, Aloe Vera Gel, Carbomer, Diisopropylamine,
Glycerin, Isopropyl Myristate, Fragrance, Phenoxyethanol, Tocopheryl Acetate, Acid Green 1

GBG AloeGel 6727 4oz

6727Z4P6318.jpg GBG AloeGel 4 oz

INGREDIENTS AND APPEARANCE

GBG ALOEGEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63843-727
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)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
NONOXYNOL-9 (UNII: 48Q180SH9T)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63843-727-06	1 in 1 BOX
1		800 mL in 1 BAG
2	NDC: 63843-727-17	532 mL in 1 BOTTLE, PLASTIC
3	NDC: 63843-727-24	115 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	07/31/2009

Labeler - HealthLink (807714126)

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

Establishment
Name	Address	ID/FEI	Business Operations
ABC Compounding Co., Inc.		003284353	manufacture