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Osceola Supply Inc 6176

Dosage form: soap
Ingredients: CHLOROXYLENOL 6mg in 1mL
Labeler: OSCEOLA SUPPLY, INC.
NDC Code: 62672-300

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.

Medicated Lotion Soap 6176 Drug Facts and Label

Drug Facts Box OTC-Active Ingredient Section

Chloroxylenol 0.6%


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, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, propylene glycol, sodium chloride, PEG-75 lanolin, sodium styrene/PEG-10 maleate/nonoxynol-10 maleate/acrylates copolymer, boric acid, fragrance, methylparaben, propylparaben, aloe barbadensis

Medicated Lotion Soap 6176 Label

Medicated Lotion Soap 61766176M4P5136.jpg

OSCEOLA SUPPLY INC 6176 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62672-300
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
COCAMIDOPROPYL BETAINE 
PROPYLENE GLYCOL 
SODIUM CHLORIDE 
ALOE VERA LEAF 
PROPYLPARABEN 
METHYLPARABEN 
BORIC ACID 
SODIUM LAURYL SULFATE 
PEG-75 LANOLIN 
Packaging
#Item CodePackage Description
1NDC:62672-300-17532 mL in 1 BOTTLE, PLASTIC
2NDC:62672-300-24118 mL in 1 BOTTLE, PLASTIC
3NDC:62672-300-011200 mL in 1 CARTRIDGE
4NDC:62672-300-03350 mL in 1 CARTRIDGE
5NDC:62672-300-05540 mL in 1 BOTTLE, PLASTIC
6NDC:62672-300-07700 mL in 1 BAG
7NDC:62672-300-092000 mL in 1 CARTRIDGE
8NDC:62672-300-101000 mL in 1 CARTRIDGE
9NDC:62672-300-111000 mL in 1 BOTTLE, PLASTIC
10NDC:62672-300-121000 mL in 1 BAG
11NDC:62672-300-13800 mL in 1 BAG
12NDC:62672-300-143785 mL in 1 BOTTLE, PLASTIC
13NDC:62672-300-15946 mL in 1 BOTTLE, PLASTIC
14NDC:62672-300-28149 mL in 1 BOTTLE, PLASTIC
15NDC:62672-300-27800 mL in 1 CARTRIDGE
16NDC:62672-300-552082 mL in 1 DRUM
17NDC:62672-300-16236 mL in 1 BOTTLE, PLASTIC
18NDC:62672-300-1850 mL in 1 BOTTLE, PLASTIC
19NDC:62672-300-191890 mL in 1 CONTAINER
20NDC:62672-300-207560 mL in 1 DRUM
21NDC:62672-300-351325 mL in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/22/2016
Labeler - OSCEOLA SUPPLY, INC. (809050479)
Registrant - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIOperations
ABC Compounding Co., Inc.003284353manufacture(62672-300)

Revised: 07/2016
 
OSCEOLA SUPPLY, 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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