Spa Sense Antibacterial Hand Wash Eucalyptus Aloe by LAB-CLEAN, INC

Spa Sense Antibacterial Hand Wash Eucalyptus Aloe by

Drug Labeling and Warnings

Spa Sense Antibacterial Hand Wash Eucalyptus Aloe by is a Otc medication manufactured, distributed, or labeled by LAB-CLEAN, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPA SENSE ANTIBACTERIAL HAND WASH EUCALYPTUS ALOE- benzalkonium chloride liquid 
LAB-CLEAN, 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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Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only!

When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

Stop use and ask a doctor if irritation or redness develops and conditions persist.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply small amount of product to wet hands. Work into lather and rinse thoroughly. Dry hands.

Inactive ingredients

Water, Cocobetaine, Sodium Coco Sulfate, Phenoxyethanol, Natural fragrance.

Package Label - Principal Display Panel

Label

SPA SENSE ANTIBACTERIAL HAND WASH EUCALYPTUS ALOE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73126-021
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
WATER (UNII: 059QF0KO0R)  
COCO-BETAINE (UNII: 03DH2IZ3FY)  
SODIUM COCO-SULFATE (UNII: 3599J29ANH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73126-021-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
2NDC: 73126-021-02474 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
3NDC: 73126-021-03709 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
4NDC: 73126-021-04946 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/01/202004/20/2024
Labeler - LAB-CLEAN, INC (199822219)
Establishment
NameAddressID/FEIBusiness Operations
LAB-CLEAN, INC199822219manufacture(73126-021)

Revised: 4/2022
 

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