WEBER RINSE FREE SKIN SANITIZER- benzalkonium chloride liquid 
Bryson Industries 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.

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Weber Rinse Free Skin Sanitizer

Drug Facts

Active Ingreident

Benzalkonium chloride 0.13%

Purpose

Antiseptic Skin Sanitizer

Uses

  • Sanitizer to help decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

For external use only.

  • Do not use in ears or mouth.

When using this product

  • Avoid contact with the eyes
  • In case of contact flush eyes with water

Stop use and ask a doctor

if redness or irritation develop and persist for more than 72 hours

Keep out of reach of children

Children should be supervised when using this product

Directions

  • Apply a small amount into palms of hands and spread on both hands.
  • Rub into skin until dry.

Inactive Ingredients

1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, 1-Octadecanaminium NN dimethyl(3-trihydroxysilyl)propylchloride, Aloe Barbadenis leaf extract, Aqua, Caprylyl glucoside, Citric acid, Laureth-4, Methylparaben, Polyaminopropyl biguanide, Silk protein

Package Labeling

weber rinse

WEBER RINSE FREE SKIN SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71853-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)  
OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDE (UNII: GLJ50K866T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
LAURETH-4 (UNII: 6HQ855798J)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71853-003-07200 mL in 1 BOTTLE; Type 0: Not a Combination Product01/22/201812/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/22/201812/31/2021
Labeler - Bryson Industries Inc (040363256)

Revised: 12/2022
Document Id: ef1b74df-7c82-8a8d-e053-2995a90a6810
Set id: faf99c22-ce60-4060-8bde-ad13d76e764d
Version: 4
Effective Time: 20221205
 
Bryson Industries Inc