United Airlines Transcon Kit

United Airlines Transcon Kit by

Drug Labeling and Warnings

United Airlines Transcon Kit by is a Otc medication manufactured, distributed, or labeled by Buzz Export Services Pty Ltd (Buzz Products). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UNITED AIRLINES TRANSCON KIT- sodium monofluorophosphate, alcohol 
Buzz Products Inc.

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United Airlines Transcon Kit

Drug Facts

Active ingredient

Sodium monofluorophosphate 0.76% (0.15% w/v fluoride ion)

Purpose

Anticavity

Use

helps protect against cavities

Warnings

Keep out of the reach of children under 6 years of age.

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

 adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician
 children 2 to 6 years use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
 children under 2 years ask a dentist or physician

Inactive ingredients

dicalcium phosphate dihydrate, water, sorbitol, sodium lauryl sulfate, flavor, cellulose gum, tetrasodium pyrophosphate, sodium saccharin

Questions or comments?

Call to-free 1-800-468-6502

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 wipes in flush toilets. 
  • Keep away from fire or flame.

Flammable

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

  • Appyl to hands or surface.
  • 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:69491-038-01

Kit4Kit2

Package Labeling:42555-060-94

Tube

Package Labeling:69491-035-01

Label0

UNITED AIRLINES TRANSCON KIT 
sodium monofluorophosphate, alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69491-038
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69491-038-011 in 1 KIT02/15/202211/30/2025
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 5 g
Part 21 PATCH 5 mL
Part 1 of 2
COLGATE ANTICAVITY 
sodium monofluorophosphate paste, dentifrice
Product Information
Item Code (Source)NDC: 42555-060
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION7.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 42555-060-945 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/15/2022
Part 2 of 2
SANITIZER WIPE IN SACHET 
alcohol cloth
Product Information
Item Code (Source)NDC: 69491-035
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
TEA TREE OIL (UNII: VIF565UC2G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69491-035-011 in 1 PACKAGE
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 Drug505G(a)(3)02/15/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/15/202211/30/2025
Labeler - Buzz Products Inc. (144902952)

Revised: 3/2026
 

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