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Clinical Works Lavender Blossom Waterless Hand Sanitizer

Dosage form: liquid
Ingredients: ALCOHOL 62.000g in 100g
Labeler: Taizhou Xinzhixuan Daily-Use Co., Ltd.
NDC Code: 50593-006

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.

Drug Fact

Active Ingredients
Ethyl Alcohol 62%



  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use


For external use only-hands. 
Flammable. Keep away from heat and flame.
When using this product, Keep out of eyes. In case of contact with eyes, flush thoroughly with water.  Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a doctor if skin irritation develops.
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


Wet hands thoroughly with product and allow to dry without wiping.
For children under 6,use only under adult supervision.
Not recommended for infants.

Other Information

Do not store above 105F
May discolor some fabrics.
Harmful to wood finishes and plastics

Inactive Ingredients

water(Aqua), Glycerin, Triethanolamine, Carbomer, Fragrance(parfum), PEG-40 Hydrogenated Castor Oil, DMDM Hydantoin, FD and C Yellow No. 5, FD and C Blue No. 1, FD and C Red No. 40


alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50593-006
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62.000 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER35.39999 g  in 100 g
GLYCERIN1.0 g  in 100 g
TROLAMINE0.25 g  in 100 g
CARBOMER 9340.25 g  in 100 g
DMDM HYDANTOIN0.4 g  in 100 g
POLYOXYL 40 CASTOR OIL0.5 g  in 100 g
FD&C YELLOW NO. 50.000003 g  in 100 g
FD&C BLUE NO. 10.000003 g  in 100 g
FD&C RED NO. 400.000004 g  in 100 g
LAVENDER0.2 g  in 100 g
#Item CodePackage Description
1NDC:50593-006-0160 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33306/10/2010
Labeler - Taizhou Xinzhixuan Daily-Use Co., Ltd. (420438920)
Registrant - Taizhou Xinzhixuan Daily-Use Co., Ltd. (420438920)
Taizhou Xinzhixuan Daily-Use Co., Ltd.420438920manufacture

Revised: 06/2010
Taizhou Xinzhixuan Daily-Use Co., Ltd.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.