INDULGENCE/PROPOWER- benzalkonium chloride soap 
U S Chemical Corporation

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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US Chem F213F

Benzalkonium Chloride 0.13% w/w

Antibacterial Agent

For handwashing to decrease bacteria on skin.

For external use only.

Avoid contact with eyes. In case of contact, flush with plenty of water.

Stop use and ask a doctor if irritation or rash appears and persists.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. ​EMERGENCY TELEPHONE: 1-866-923-4913

To decrease bacteria on skin, apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

Water, cocamidopropyl betaine, cocamidopropyl PG-dimonium chloride phosphate, PEG-6 cocamide, laurtrimonium chloride, aloe barbadensis leaf juice, tocopheryl acetate (vitamin E), fragrance, iodopropynyl butylcarbamate, methylisothiazolinone, yellow 5, red 33.

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INDULGENCE/PROPOWER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61307-213
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE2.5 mg  in 1 L
Inactive Ingredients
Ingredient NameStrength
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61307-213-411 L in 1 BAG; Type 0: Not a Combination Product01/30/2017
2NDC:61307-213-101 L in 1 BAG; Type 0: Not a Combination Product01/30/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/30/2017
Labeler - U S Chemical Corporation (031457842)
Establishment
NameAddressID/FEIBusiness Operations
Kutol Products Company004236139manufacture(61307-213)

Revised: 8/2023
Document Id: 03a8d733-d4d1-c48f-e063-6294a90a8621
Set id: 47556b9b-cd84-6385-e054-00144ff8d46c
Version: 16
Effective Time: 20230824
 
U S Chemical Corporation