ZERO-DUST DAYS HAND SANITIZER by MOTHER-K CO.,LTD / DONG IL PHARMS CO., LTD. Drug Facts

ZERO-DUST DAYS HAND SANITIZER by

Drug Labeling and Warnings

ZERO-DUST DAYS HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by MOTHER-K CO.,LTD, DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZERO-DUST DAYS HAND SANITIZER- alcohol liquid 
MOTHER-K CO.,LTD

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 Facts

Alcohol

Water
Alcohol
Aloe Barbadensis Leaf Juice
Butylene Glycol
Citrus Paradisi (Grapefruit) Fruit Extract
Citrus Aurantium Dulcis (Orange) Oil
Hydrolyzed Collagen Extract

Antiseptic

KEEP OUT OF REACH OF THE CHILDREN

For the external use only

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

No dilution is required. Use it by immersing or spraying it where you want. No additional cleaning process is required after use.

1

ZERO-DUST DAYS HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73429-0003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73429-0003-1500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/202004/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/01/202004/02/2020
Labeler - MOTHER-K CO.,LTD (689540220)
Registrant - MOTHER-K CO.,LTD (689540220)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(73429-0003)
Establishment
NameAddressID/FEIBusiness Operations
MOTHER-K CO.,LTD689540220label(73429-0003)

Revised: 4/2020
Document Id: a24ab61d-5252-569d-e053-2995a90ab643
Set id: a2487928-4004-c6d8-e053-2a95a90a21c2
Version: 2
Effective Time: 20200402
 
MOTHER-K CO.,LTD