Foamy Mango Antiseptic Hand and Body Wash 6876 Drug facts and Label

Foamy Mango Antiseptic Hand and Body Wash by

Drug Labeling and Warnings

Foamy Mango Antiseptic Hand and Body Wash by is a Otc medication manufactured, distributed, or labeled by ABC Compounding Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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Foamy Mango Antiseptic Hand and Body Wash 6876 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

  • 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, DMDM hydantoin, fragrance, methylchloroisothiazolinone, methylisothiazolinone, aloe barbadensis, acid red 1

Foamy Mango Antiseptic Hand and Body Wash 6876

product label

Foamy Mango Antiseptic Hand and Body Wash 6876

FOAMY MANGO ANTISEPTIC HAND AND BODY WASH 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 62257-976
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)  
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: 62257-976-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
2NDC: 62257-976-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/2017
3NDC: 62257-976-121000 mL in 1 BAG; Type 0: Not a Combination Product01/04/2017
4NDC: 62257-976-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/2017
5NDC: 62257-976-55208200 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 DrugM00301/04/201711/19/2025
Labeler - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIBusiness Operations
ABC Compounding Co., Inc.003284353manufacture(62257-976)

Revised: 11/2025
Document Id: 43f88237-7e3e-f601-e063-6394a90a5d5c
Set id: 0f2a88e4-723a-19c7-e063-6294a90aa935
Version: 2
Effective Time: 20251119