SURGENT ANTISEPTIC- chloroxylenol soap 
SunCoast Paper Inc.

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.

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Surgent Antiseptic Hand Soap 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 Section

Drug Facts Box OTC-Inactive Ingredient Section

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

Surgent Antiseptic Hand Soap 800 mL  

product label

Surgent Antiseptic Hand Soap 800 mL  

SURGENT ANTISEPTIC 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66155-544
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66155-544-061 in 1 BOX10/12/2015
1800 mL in 1 BAG; Type 0: Not a Combination Product
2NDC:66155-544-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
3NDC:66155-544-24118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
4NDC:66155-544-011200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/12/2015
5NDC:66155-544-03350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/12/2015
6NDC:66155-544-05540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
7NDC:66155-544-07700 mL in 1 BAG; Type 0: Not a Combination Product10/12/2015
8NDC:66155-544-092000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/12/2015
9NDC:66155-544-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/12/2015
10NDC:66155-544-111000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
11NDC:66155-544-121000 mL in 1 BAG; Type 0: Not a Combination Product10/12/2015
12NDC:66155-544-13800 mL in 1 BAG; Type 0: Not a Combination Product10/12/2015
13NDC:66155-544-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
14NDC:66155-544-15946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
15NDC:66155-544-28149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
16NDC:66155-544-27800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/12/2015
17NDC:66155-544-55208200 mL in 1 DRUM; Type 0: Not a Combination Product10/12/2015
18NDC:66155-544-081 in 1 BOX10/12/2015
181000 mL in 1 BAG; Type 0: Not a Combination Product
19NDC:66155-544-16236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
20NDC:66155-544-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/12/2015
21NDC:66155-544-1918900 mL in 1 CONTAINER; Type 0: Not a Combination Product10/12/2015
22NDC:66155-544-2075600 mL in 1 DRUM; Type 0: Not a Combination Product10/12/2015
23NDC:66155-544-35132500 mL in 1 DRUM; Type 0: Not a Combination Product10/12/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/2012
Labeler - SunCoast Paper Inc. (031211089)
Registrant - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIBusiness Operations
ABC Compounding Co., Inc.003284353manufacture(66155-544)

Revised: 12/2018
Document Id: 36e7ee81-dfe3-40bf-95ea-d215ccdf413a
Set id: c8cea8f7-8f51-4dc7-99e3-aca786b9ca67
Version: 2
Effective Time: 20181227
 
SunCoast Paper Inc.