SPA SENSE HAND SANITIZER Eucalyptus Lavender

SPA SENSE HAND SANITIZER Eucalyptus Lavender by

Drug Labeling and Warnings

SPA SENSE HAND SANITIZER Eucalyptus Lavender by is a Otc medication manufactured, distributed, or labeled by LAB-CLEAN, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPA SENSE HAND SANITIZER EUCALYPTUS LAVENDER- 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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SPA SENSE HAND SANITIZER Eucalyptus Lavender

Active Ingredients

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Warnings

For external use only!

When using this product avoid contact with eyes.

In case of eye contact, flush eyes with water.

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

Uses

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

Directions

  • Spray a small amount of product into palm of hand. Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive ingredients

Water, Cetrimonium chloride, laurtrimonium chloride, Dihydroxyethyl Cocamine Oxide, glycereth-17 cocoate, citric acid, fragrance

Package

image description

SPA SENSE HAND SANITIZER EUCALYPTUS LAVENDER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73126-012
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)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73126-012-0159 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
2NDC: 73126-012-0288 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
3NDC: 73126-012-03236 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
4NDC: 73126-012-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
5NDC: 73126-012-05355 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
6NDC: 73126-012-06474 mL in 1 PACKAGE; Type 0: Not a Combination Product06/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/11/202004/20/2024
Labeler - LAB-CLEAN, INC (199822219)
Establishment
NameAddressID/FEIBusiness Operations
LAB-CLEAN, INC199822219manufacture(73126-012)

Revised: 4/2022
Document Id: dd93f75e-9f90-e2b4-e053-2a95a90ab3d3
Set id: 1ba75762-3bed-4e99-b548-a1bec0740ea7
Version: 4
Effective Time: 20220426
 
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