Dr. Pure Antiseptic Liquid Hand Soap, Coconut and Honey Scented

Dr. Pure Antiseptic Liquid Hand Soap, Coconut and Honey Scented by

Drug Labeling and Warnings

Dr. Pure Antiseptic Liquid Hand Soap, Coconut and Honey Scented by is a Otc medication manufactured, distributed, or labeled by Industrias Bernal Canton S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. PURE ANTISEPTIC LIQUID HAND SOAP, COCONUT AND HONEY SCENTED- benzalkonium chloride liquid 
Industrias Bernal Canton S.A. de C.V.

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.

----------

Dr. Pure Antiseptic Liquid Hand Soap, Coconut and Honey Scented

Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only.

Do not use

in the eyes.

Stop use and ask a doctor 

irritation and redness develop

condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet hands and forearms.
  • Apply palmful to hands and forearms.
  • Scrub thoroughly.
  • Rinse and repeat

Inactive ingredients

Water, sodium laureth sulfate, sodium chloride, cocamidopropyl betaine, glycol distearate, DMDM hydantoin, glycerol, honey extract, aloe vera (aloe barbadensis) leaf extract, fragrance,

Package Labeling:

Bottle

DR. PURE ANTISEPTIC LIQUID HAND SOAP, COCONUT AND HONEY SCENTED 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78239-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERIN (UNII: PDC6A3C0OX)  
HONEY (UNII: Y9H1V576FH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78239-002-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/09/202104/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/09/202104/01/2023
Labeler - Industrias Bernal Canton S.A. de C.V. (812827340)

Revised: 3/2023
Document Id: f76c17df-b007-c522-e053-6294a90a5509
Set id: bfde0148-77eb-0dd7-e053-2995a90ab9d5
Version: 2
Effective Time: 20230321