Label: BRUSH BUDDIES SENSITIVE EXTRA WHITENING- potassium nitrate, sodium fluoride paste, dentifrice
- NDC Code(s): 70108-079-01
- Packager: Ashtel Studios, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated September 26, 2023
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- Drug Facts
- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
• adults and children 12 years & older: • apply at least a 1-inch strip of the product onto a soft bristle toothbrush
• brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist. Make sure to brush all sensitive areas of the teeth.
• minimize swallowing. Spit out after brushing.
• children under 12 years of age: Consult a dentist or doctor. - Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
TOOTHPASTE FOR SENSITIVE TEETH AND CAVITY PREVENTION
FRESH MINT
• FRESHENS BREATH
• STRENGTHENS TEETH WITH ACTIVE FLUORIDECompares to the active ingredients in Sensodyne® Extra Whitening*
*This product is not manufactured or distributed by GSK Consumer Healthcare, owner of the registered trademark Sensodyne®.
DESIGNED IN U.S.A. • MADE IN INDIA
Brush Buddies®
WWW.BRUSHBUDDIES.COMQUESTIONS OR COMMENTS?
1-877-274-8358 TOLL FREE IN USA
1-909-434-0911 INTERNATIONALPATENTS, COPYRIGHTS & TRADEMARKS GRANTED OR PENDING WORLDWIDE
DISTRIBUTED BY ASHTEL STUDIOS INC.
ONTARIO, CALIFORNIA 91761 - Packaging
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INGREDIENTS AND APPEARANCE
BRUSH BUDDIES SENSITIVE EXTRA WHITENING
potassium nitrate, sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70108-079 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE 5 g in 100 g SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 0.24 g in 100 g Inactive Ingredients Ingredient Name Strength SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) WATER (UNII: 059QF0KO0R) POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Product Characteristics Color Score Shape Size Flavor MINT (Fresh mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70108-079-01 1 in 1 BOX 09/07/2023 1 113 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M022 09/07/2023 Labeler - Ashtel Studios, Inc. (148689180)