Label: ADVANCE WHITE EXTREME WHITENING TARTAR CONTROL- sodium fluoride paste, dentifrice
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NDC Code(s):
10237-658-09,
10237-658-12,
10237-658-43,
10237-658-60, view more10237-658-72
- Packager: Church & Dwight Co., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 22, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions do not swallow supervise children as necessary until capable of using without supervision
rinse away toothpaste residue throughly after brushingadults and children 2 years and older brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician
children under 6 years instruct in good brushing and rinsing habits (to minimize swallowing)
children under 2 years ask a dentist or physician - INACTIVE INGREDIENT
- QUESTIONS
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ADVANCE WHITE EXTREME WHITENING TARTAR CONTROL
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10237-658 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 2.4 mg in 1 g Inactive Ingredients Ingredient Name Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLOXALENE (UNII: V8B3K56SW0) SODIUM PERCARBONATE (UNII: Z7G82NV92P) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SACCHARIN SODIUM (UNII: SB8ZUX40TY) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) Product Characteristics Color WHITE Score Shape Size Flavor MINT (Fresh Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10237-658-09 1 in 1 CARTON 01/29/2012 1 25 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10237-658-43 1 in 1 CARTON 01/29/2012 2 121 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:10237-658-60 1 in 1 CARTON 01/29/2012 3 170 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:10237-658-72 1 in 1 CARTON 01/29/2012 12/31/2024 4 204 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:10237-658-12 2 in 1 CARTON 09/23/2019 12/31/2024 5 340 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 DRUG M021 01/29/2012 Labeler - Church & Dwight Co., Inc. (001211952) Establishment Name Address ID/FEI Business Operations Church & Dwight Co., Inc. 043690812 MANUFACTURE(10237-658)