Gold and Sudsy

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.003mg in 1mL
Labeler: Cosgrove Enterprises, Inc.
NDC Code: 52674-544

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Gold & Sudsy 6544 Drug Facts and Label

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 Sectionwet 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 DEA, propylene glycol, sodium chloride, citric acid, fragrance, hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine, acid yellow 36, acid red 1

Gold & Sudsy 6544 800 ml

6544M4P6218.jpg  Gold and Sudsy  800 ml 

GOLD AND SUDSY 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52674-544
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
SODIUM LAURETH SULFATE 
CITRIC ACID MONOHYDRATE 
METANIL YELLOW 
SODIUM CHLORIDE 
DECYL GLUCOSIDE 
COCO DIETHANOLAMIDE 
Packaging
#Item CodePackage Description
1NDC:52674-544-061 BAG (BAG) in 1 BOX
1800 mL in 1 BAG
2NDC:52674-544-17532 mL in 1 BOTTLE, PLASTIC
3NDC:52674-544-24118 mL in 1 BOTTLE, PLASTIC
4NDC:52674-544-011200 mL in 1 CARTRIDGE
5NDC:52674-544-03350 mL in 1 CARTRIDGE
6NDC:52674-544-05540 mL in 1 BOTTLE, PLASTIC
7NDC:52674-544-07700 mL in 1 BAG
8NDC:52674-544-092000 mL in 1 CARTRIDGE
9NDC:52674-544-101000 mL in 1 CARTRIDGE
10NDC:52674-544-111000 mL in 1 BOTTLE, PLASTIC
11NDC:52674-544-121000 mL in 1 BAG
12NDC:52674-544-13800 mL in 1 BAG
13NDC:52674-544-143785 mL in 1 BOTTLE, PLASTIC
14NDC:52674-544-15946 mL in 1 BOTTLE, PLASTIC
15NDC:52674-544-28149 mL in 1 BOTTLE, PLASTIC
16NDC:52674-544-27800 mL in 1 CARTRIDGE
17NDC:52674-544-55208200 mL in 1 DRUM
18NDC:52674-544-081 BAG (BAG) in 1 BOX
181000 mL in 1 BAG
19NDC:52674-544-16236 mL in 1 BOTTLE, PLASTIC
20NDC:52674-544-1850 mL in 1 BOTTLE, PLASTIC
21NDC:52674-544-1918900 mL in 1 CONTAINER
22NDC:52674-544-2075600 mL in 1 DRUM
23NDC:52674-544-35132500 mL in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2011
Labeler - Cosgrove Enterprises, Inc. (056128473)
Registrant - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIOperations
ABC Compounding Co., Inc.003284353manufacture

Revised: 06/2011
 
Cosgrove Enterprises, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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