glanHealth - Sanitizing Bath Wipe Advanced

glanHealth Sanitizing Bath Wipe Advanced by

Drug Labeling and Warnings

glanHealth Sanitizing Bath Wipe Advanced by is a Otc medication manufactured, distributed, or labeled by Dalrada Health Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GLANHEALTH SANITIZING BATH WIPE ADVANCED- benzalkonium chloride cloth 
Dalrada Health Products

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glanHealth - Sanitizing Bath Wipe Advanced

DIRECTIONS FOR USE:

WIPE LIBERALLY OVER THE HANDS AND BODY, RUB INTO SKIN UNTIL DRY. RECOMMENDED FOR SINGLE USE.

ACTIVE INGREDIENT:

Benzalkonium Chloride 0.13%

PURPOSE:

Antiseptic / hand and skin sanitizer

USES:

Cleans and sanitizes the skin and dcreases bacteria. Recommended for single use.

INACTIVE INGREDIENTS:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

WARNINGS:

DO NOT FREEZE. FOR EXTERNAL USE ONLY.  

DO NOT USE

IN EARS, EYES, OR MOUTH.

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

Stop use and ask a doctor 

if redness or irritation develops and persists for more than 72 hours

Keep out of reach fo children

  • Children should be supervised when using this product.

QUESTIONS?

1(855) 862-1526, Mon-Fri 9:00AM-5:00PM (CST)

Package Labeling:

Label2

GLANHEALTH SANITIZING BATH WIPE ADVANCED 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 77071-010
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
LAURETH-4 (UNII: 6HQ855798J)  
POLIHEXANIDE (UNII: 322U039GMF)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 77071-010-001 in 1 PACKET01/01/202003/02/2023
124.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/01/202003/02/2023
Labeler - Dalrada Health Products (116754421)

Revised: 12/2023