United Airlines Sanitizer Wipe

United Airlines Sanitizer Wipe by

Drug Labeling and Warnings

United Airlines Sanitizer Wipe by is a Otc medication manufactured, distributed, or labeled by Buzz Products (HK) Co. Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UNITED AIRLINES SANITIZER WIPE- alcohol cloth 
Buzz Products (HK) Co. Limited

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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United Airlines Sanitizer Wipe

Drug Facts

Active Ingredient

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

  • To help reduce bacteria on the skin.

Warnings

  • For external use only.
  • Do not dispose of wipe 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 surfaces.
  • No rinsing required.
  • Discard after use.

Other Information

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

Aqua (Water), Glycerin, Polyquaternium-37, Melaleuca Alternifolia Leaf Oil.

Package Labeling:

Bottle

UNITED AIRLINES SANITIZER WIPE 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70402-256
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
TEA TREE OIL (UNII: VIF565UC2G)  
POLYQUATERNIUM-37 (25000 MPA.S) (UNII: 31L31U8285)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70402-256-011 in 1 POUCH01/11/202112/31/2021
15 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 finalpart333E01/11/202112/31/2021
Labeler - Buzz Products (HK) Co. Limited (663516515)

Revised: 12/2021
Document Id: d42324e1-981a-16d8-e053-2a95a90a5255
Set id: b7b1e9f7-8ef2-92d4-e053-2a95a90ad4fd
Version: 2
Effective Time: 20211227