Travelshield Sanitizing Wipes 70%

Travelshield Sanitizing Wipes 70 by

Drug Labeling and Warnings

Travelshield Sanitizing Wipes 70 by is a Otc medication manufactured, distributed, or labeled by WESSCO International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TRAVELSHIELD SANITIZING WIPES 70- alcohol cloth 
WESSCO International

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.

----------

Travelshield Sanitizing Wipes 70%

Drug Facts

Active Ingredient:

Ethyl Alcohol 80%

Purpose

Antimicrobial

Uses:

To help reduce microbes on the skin

Warnings

  • For external use only
  • Do not dispose of wipes in flush toilets

Flammable: Keep away from fire or flame

When using this product:

avoid contact with eyes, If contact occurs, rinse thoroughly with water.

Stop using and ask a doctor if:

irritation or redness develops and lasts.

Keep out of reach of children:

In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

Apply to hands or skin.

No rinsing required. Discard after use.

Inactive Ingredients

Water(Aqua)

Other information:

  • Store below 110 °F (43°C)
  • May discolorcertan fabrics or surfaces

Package Labeling:100pc

100pc Box

Package Labeling:1pc

1pc Drug Facts1pc Front

TRAVELSHIELD SANITIZING WIPES 70 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 42509-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 42509-003-01100 in 1 BOX07/01/202012/31/2021
11 in 1 PACKET
12.8 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC: 42509-003-021 in 1 PACKET07/01/202012/31/2021
22.8 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 finalpart333E07/01/202012/31/2021
Labeler - WESSCO International (118553619)

Revised: 4/2023
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.