SANI MANGO ANTISEPTIC HAND AND BODY WASH- chloroxylenol soap 
ABC Compounding Co., 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.

----------

Sani Mango Antiseptic Hand and Body Wash 6875 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, methylchloroisothiazolinone, methylisothiazolinone, DMDM hydantoin, fragrance, aloe barbadensis, acid red 1

Sani Mango Antiseptic Hand and Body Wash 6875

product label

Sani Mango Antiseptic Hand and Body Wash

SANI MANGO ANTISEPTIC HAND AND BODY WASH 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-875
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)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ACID RED 1 (UNII: 3365R6427R)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62257-875-061 in 1 BOX01/04/2017
1800 mL in 1 BAG; Type 0: Not a Combination Product
2NDC:62257-875-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
3NDC:62257-875-24118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
4NDC:62257-875-011200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
5NDC:62257-875-03350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
6NDC:62257-875-05540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
7NDC:62257-875-07700 mL in 1 BAG; Type 0: Not a Combination Product01/04/2017
8NDC:62257-875-092000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
9NDC:62257-875-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
10NDC:62257-875-111000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
11NDC:62257-875-121000 mL in 1 BAG; Type 0: Not a Combination Product01/04/2017
12NDC:62257-875-13800 mL in 1 BAG; Type 0: Not a Combination Product01/04/2017
13NDC:62257-875-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
14NDC:62257-875-15946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
15NDC:62257-875-28149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
16NDC:62257-875-27800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
17NDC:62257-875-55208200 mL in 1 DRUM; Type 0: Not a Combination Product01/04/2017
18NDC:62257-875-081 in 1 BOX01/04/2017
181000 mL in 1 BAG; Type 0: Not a Combination Product
19NDC:62257-875-16236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
20NDC:62257-875-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
21NDC:62257-875-1918900 mL in 1 CONTAINER; Type 0: Not a Combination Product01/04/2017
22NDC:62257-875-2075600 mL in 1 DRUM; Type 0: Not a Combination Product01/04/2017
23NDC:62257-875-35132500 mL in 1 DRUM; Type 0: Not a Combination Product01/04/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/04/2017
Labeler - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIBusiness Operations
ABC Compounding Co., Inc.003284353manufacture(62257-875)

Revised: 1/2019
Document Id: 46428e18-9344-4169-a239-04f6d8509abc
Set id: 29496844-08e6-456d-aa7b-9eb5c866fd87
Version: 2
Effective Time: 20190110
 
ABC Compounding Co., Inc.