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Fluoride Foam: Package Insert / Prescribing Info

Package insert / product label
Dosage form: aerosol, foam
Drug class: Mouth and throat products

Medically reviewed by Drugs.com. Last updated on Mar 25, 2024.

Indications: For the topical application of fluoride to aid in the
protection against dental caries.

Contraindications: This product should not be used with
individuals with known sensitivities to fluoride.

Directions for Use:
1. Remove cap from can.
2. The first time you dispense from a new can, gently lift upward
on the nozzle to break the protective shipping tab (Fig. 1).
3. Shake can vigorously for at least 10 seconds before each use.
4. Hold can completely upside down to dispense (Fig. 2).
5. Point can towards applicator tray and slowly press the nozzle
to fill tray. Use one press per arch, as foam will expand
slightly to fill the tray.
6. For best results, dry teeth prior to application.
7. Insert the filled tray and have the patient bite down lightly,
with a chewing motion to ensure interproximal coverage.
8. Leave tray(s) in contact with teeth for 1 to 4 minutes.
9. Use a saliva ejector during treatment to minimize ingestion
of product.
10. Remove tray(s) and have patient expectorate.
11. Instruct patient not to eat, drink, or rinse for at least 30
minutes after application.
Contains:
1.23% Fluoride ion from sodium fluoride in a proprietary
acidulated phosphate flavored foam base. Does not contain
chlorofluorocarbon propellant.
Sweetened with Xylitol (sucralose). Does not contain Aspartame
or Saccharin. Gluten free.
Precautions:
Use only as directed.
For dental use only. U.S. Federal Law prohibits dispensing
without prescription.
Not for unsupervised home use. Safety and efficacy in patients
under the age of 3 has not been established. Repeated use of
APF formulations in patients with porcelain or composite
restorations should be avoided due to the possibility of etching
the restoration surface.
Warning:
Do not swallow.
Keep out of reach of children.
Avoid spraying toward open flame.
Contents under pressure.
Do not puncture or incinerate.
WATERPIK
Ultra Control
Fluoride Foam
MINT

Precise foaming action
Sweetened with Xylitol
Gluten free

*Acidulated Phosphate Fluoride
1.23% Fluoride Ion (pH 3.5)

For professional use only.
Store at room temperature
between 55°–80°F.
Shake well before each use.

To obtain a MSDS sheet, please
call Water Pik, Inc. customer
service at 1-800-525-2020.
Made in the U.S.A.
Distributed by:
Water Pik, Inc.
1730 E. Prospect Road
Fort Collins, CO 80553-0001
1-800-525-2020
www.waterpik.com
Waterpik® (stylized) is a
trademark of Water Pik, Inc.
registered Canada, EU, Japan,
Mexico, Switzerland, and the
United States.
©2011 Water Pik, Inc.
Water Pik Item Number:
20014143
FN 20014519-F AA
373485

UltraControl Foam ART Mint-Carton_BK

UltraControl Foam ART Mint-Carton_FR
UltraControl Foam ART Mint-LBL
FLUORIDE MINT
sodium fluoride aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:75905-003
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.23 g in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XYLITOL (UNII: VCQ006KQ1E)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
BETAINE (UNII: 3SCV180C9W)
POLOXAMER 407 (UNII: TUF2IVW3M2)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75905-003-14125 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/20/2011
Labeler - WATER PIK, INC. (001804074)
Registrant - WATER PIK, INC. (001804074)