Dynamics Hand Sanitizing Alcohol Wipes

Dynamics Hand Sanitizing Alcohol Wipes by

Drug Labeling and Warnings

Dynamics Hand Sanitizing Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by MILKY WAY INTERNATIONAL TRADING CORP, Kangna (Zhejiang) Medical Supplies Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DYNAMICS HAND SANITIZING ALCOHOL WIPES- alcohol cloth 
MILKY WAY INTERNATIONAL TRADING CORP

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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Dynamics Hand Sanitizing Alcohol Wipes

Drug Facts

Active Ingredient

Alcohol 75% by volume

Purpose

Antiseptic

Uses

  • For hand sanitizing to decrease bacteria on the skin.
  • Apply topically to the skin to help prevent cross contamination.
  • Not recommended for repeated use.
  • Dries in seconds.

Warnings

  • Flammable, Keep away from fire or flame. For external use only.

Do not use 

in or contact the eyes.

Stop use and ask a doctor if

  • too much skin irritation or sensitivity develops or increases.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • Open lid, gently pull back resealable label, remove and use wipe as requited.
  • Reseal back after use to avoid evaporation of alcohol.

Other informations

  • Store at room temperature 15°-30°C (59°-86°F).
  • Lot No. Manufacture date and Expiration date can be found on package.

Inactive Ingredient

Water.

Package Labeling:

Bottle

DYNAMICS HAND SANITIZING ALCOHOL WIPES 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79203-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79203-000-0050 in 1 BAG07/01/202012/31/2022
14.76 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 not finalpart333E07/01/202012/31/2022
Labeler - MILKY WAY INTERNATIONAL TRADING CORP (083898916)

Revised: 12/2022
Document Id: f0d5263e-6094-77b2-e053-2995a90a0ff0
Set id: c400ea3a-6a6c-488e-b132-a43333301329
Version: 4
Effective Time: 20221227