Label: WHITE GLO CHARCOAL SENSITIVE- potassium nitrate, sodium monofluorophosphate kit
- NDC Code(s): 73656-011-00, 73656-012-00
- Packager: WHITE GLO USA INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 31, 2023
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- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
• adults and children 12 years of age and older: • apply at least a 1-inch strip of the product onto a soft bristle toothbrush. • brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by dentist or doctor. 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.
- Other information
- Inactive ingredients
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
WHITE GLO CHARCOAL SENSITIVE
potassium nitrate, sodium monofluorophosphate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73656-011 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-011-00 1 in 1 KIT 03/16/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOX 150 g Part 1 of 1 WHITE GLO CHARCOAL SENSITIVE
potassium nitrate, sodium monofluorophosphate paste, dentifriceProduct Information Item Code (Source) NDC:73656-012 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE 50 mg in 1 g SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 50 mg in 1 g Inactive Ingredients Ingredient Name Strength SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73656-012-00 1 in 1 TUBE 1 150 g in 1 BOX; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 03/16/2020 Labeler - WHITE GLO USA INC (117345666)