CWGC (as PLD) - DELICARE NON-ALCOHOL HAND SANITIZER (70415-503) - DELIST

DELICARE NON-ALCOHOL HAND SANITIZER by

Drug Labeling and Warnings

DELICARE NON-ALCOHOL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DELICARE NON-ALCOHOL HAND SANITIZER- benzalkonium chloride solution 
CWGC LA Inc.

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CWGC (as PLD) - DELICARE NON-ALCOHOL HAND SANITIZER (70415-503) - DELIST

Active ingredient

BENZALKONIUM CHLORIDE  0.13%

Purpose

Antibacterial

Uses

  • FOR SANITIZING TO REDUCE BACTERIA ON THE SKIN

Warnings

For external use only

WHEN USING THIS PRODUCT

  • Avoid contact with eyes. In case of eye contact, flush eyes with water.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Directions

  • Apply one shot of foaming sanitizer to dry hands.
  • Rub into skin.
  • No rinsing required.

Inactive ingredients

WATER, PROPYLENE GLYCOL, COCAMIDOPROPYL BETAINE, COCAMINE OXIDE, DISODIUM EDTA, DMDM HYDANTOIN, TRIETHANOLAMINE, FRAGRANCE, FD&C YELLOW NO. 5, FD&C BLUE NO. 1

Delicare - Non-alchol sanitizer - 007-56828-DEL

DELICARE NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70415-503
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
TROLAMINE (UNII: 9O3K93S3TK)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70415-503-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product12/21/202012/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00312/21/202012/31/2022
Labeler - CWGC LA Inc. (034967904)

Revised: 9/2023
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