ANTIBACTERIAL- chloroxylenol soap

Antibacterial by

Drug Labeling and Warnings

Antibacterial 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

Chloroxylenol 0.3%

Drug Facts Box OTC-Purpose Section

Antiseptic

Drug Facts Box OTC-Indications & Usage Section

for hand-washing to decrease bacteria on the skin

Drug Facts Box OTC-Warnings Section

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 and forearms
• apply 5 milliliters (teaspoonful) or palmful to hands and forearms
• scrub thoroughly for 1 minute and rinse

Drug Facts Box OTC-Inactive Ingredient Section

water, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, sodium chloride, citric acid, fragrance, FD and C yellow no.5, food red 10

Antibacterial 1200 ml

6544N3PA.jpg  Antibacterial 1200 ml 

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62257-770
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62257-770-06	1 in 1 BOX
1		800 mL in 1 BAG
2	NDC: 62257-770-17	532 mL in 1 BOTTLE, PLASTIC
3	NDC: 62257-770-24	118 mL in 1 BOTTLE, PLASTIC
4	NDC: 62257-770-01	1200 mL in 1 CARTRIDGE
5	NDC: 62257-770-03	350 mL in 1 CARTRIDGE
6	NDC: 62257-770-05	540 mL in 1 BOTTLE, PLASTIC
7	NDC: 62257-770-07	700 mL in 1 BAG
8	NDC: 62257-770-09	2000 mL in 1 CARTRIDGE
9	NDC: 62257-770-10	1000 mL in 1 CARTRIDGE
10	NDC: 62257-770-11	1000 mL in 1 BOTTLE, PLASTIC
11	NDC: 62257-770-12	1000 mL in 1 BAG
12	NDC: 62257-770-13	800 mL in 1 BAG
13	NDC: 62257-770-14	3785 mL in 1 BOTTLE, PLASTIC
14	NDC: 62257-770-15	946 mL in 1 BOTTLE, PLASTIC
15	NDC: 62257-770-28	149 mL in 1 BOTTLE, PLASTIC
16	NDC: 62257-770-27	800 mL in 1 CARTRIDGE
17	NDC: 62257-770-55	208200 mL in 1 DRUM
18	NDC: 62257-770-08	1 in 1 BOX
18		1000 mL in 1 BAG
19	NDC: 62257-770-16	236 mL in 1 BOTTLE, PLASTIC
20	NDC: 62257-770-18	50 mL in 1 BOTTLE, PLASTIC
21	NDC: 62257-770-19	18900 mL in 1 CONTAINER
22	NDC: 62257-770-20	75600 mL in 1 DRUM
23	NDC: 62257-770-35	132500 mL in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/09/2014

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

Establishment
Name	Address	ID/FEI	Business Operations
ABC Compounding Co., Inc.		003284353	manufacture(62257-770)