FIREFLY ANGRY BIRDS FLUORIDE- sodium fluoride aerosol, foam 
Dr. Fresh, LLC

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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Firefly Angry Birds Fluoride ToothFoam

Drug Facts

Active Ingredient

Sodium fluoride 0.243%

(0.15% w/v Fluoride ion)

Purpose

Anticavity

Uses

Helps protect against cavities

Warnings

Keep out of reach of children

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 per day, or as directed by a dentist or a physician - Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing) - Shake before use - Squirt once in your mouth or evenly on your toothbrush and brush - Supervise children as necessary until capable of using without supervision - Children under 2 years of age consult a dentist or physician

Inactive Ingredients

Aloe vera, citric acid, cocamidopropyl betaine, flavor, glycerin, menthol, poloxamer 407, purified water, silica, sodium benzoate, sodium hexametaphosphate, sucralose, tetrasodium pyrophosphate, xanthan gum, xylitol

Product Labeling

Firefly Squirt 'n' Brush Fluoride foam toothpaste

Angry Birds

Bubble gum flavor

MADE IN USA

Less Mess!

Angry Birds Toothpaste
FIREFLY ANGRY BIRDS FLUORIDE 
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64893-365
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
WATER (UNII: 059QF0KO0R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
XANTHAN GUM (UNII: TTV12P4NEE)  
XYLITOL (UNII: VCQ006KQ1E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64893-365-1545 mL in 1 BOTTLE; Type 0: Not a Combination Product05/29/201209/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35505/29/201209/01/2016
Labeler - Dr. Fresh, LLC (117376803)

Revised: 9/2021
 
Dr. Fresh, LLC