ALOEGUARD- chloroxylenol soap

AloeGuard by

Drug Labeling and Warnings

AloeGuard 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

Chloroxylenol 0.5% w/w

Drug Facts Box OTC-Purpose Section

Antimicrobial

Drug Facts Box OTC-Indications & Usage Section

Specially formulated for the sensitive skin of today's healthcare professional

broad-spectrum antimicrobial hand cleaner

for repeated washings on a daily basis

Drug Facts Box OTC-Warnings Section

For external use only

Drug Facts Box OTC-When Using Section

do not use in or near eyes

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

wet hands

apply AloeGuard

wash hands vigorously

rinse thoroughly

Drug Facts Box OTC-General Precautions Section

store at room temperature

Drug Facts Box OTC-Inactive Ingredient Section

Water, TEA lauryl sulfate, Cocamide DEA, Urea, Aloe vera gel, Fragrance, Polyquaternium 7, Glycol Stearate, DMDM hydantoin, Sodium chloride, Methyl paraben, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Propyl paraben, FDC Blue 1, FDC Green 8, FDC Orange 4

AloeGuard 6729 18oz

672918P6318.jpg   AloeGuard 18oz

INGREDIENTS AND APPEARANCE

ALOEGUARD 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63843-729
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.005 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
DIGLYCOL STEARATE (UNII: 94YQ11Y95F)
TROLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
UREA (UNII: 8W8T17847W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
D&C GREEN NO. 8 (UNII: I2W85YOX9L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63843-729-06	1 in 1 BOX
1		800 mL in 1 BAG
2	NDC: 63843-729-17	532 mL in 1 BOTTLE, PLASTIC
3	NDC: 63843-729-14	3785 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