NDC 0135-0525

Sensodyne Extra Whitening

Potassium Nitrate And Sodium Fluoride

Sensodyne Extra Whitening is a Dental Paste in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Potassium Nitrate; Sodium Fluoride.

• Product ID: 0135-0525_38529353-3b28-4a02-b2d7-54209276fc78
• NDC: 0135-0525
• Product Type: Human Otc Drug
• Proprietary Name: Sensodyne Extra Whitening
• Generic Name: Potassium Nitrate And Sodium Fluoride
• Dosage Form: Paste
• Route of Administration: DENTAL
• Marketing Start Date: 1990-09-30
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Substance Name: POTASSIUM NITRATE; SODIUM FLUORIDE
• Active Ingredient Strength: 50 mg/g; mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0135-0525-03

2 CARTON in 1 CARTON (0135-0525-03) > 1 TUBE in 1 CARTON > 113 g in 1 TUBE

• Marketing Start Date: 1990-09-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0135-0525-03 [00135052503]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-05 [00135052505]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-13 [00135052513]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-06-23

NDC 0135-0525-07 [00135052507]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-09 [00135052509]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2013-09-30

NDC 0135-0525-11 [00135052511]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-04 [00135052504]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-06 [00135052506]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-09-30

NDC 0135-0525-08 [00135052508]

Sensodyne Extra Whitening PASTE

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM NITRATE	50 mg/g

NDC Crossover Matching brand name "Sensodyne Extra Whitening" or generic name "Potassium Nitrate And Sodium Fluoride"

NDC	Brand Name	Generic Name
0135-0525	Sensodyne	potassium nitrate and sodium fluoride
0135-0526	Sensodyne	potassium nitrate and sodium fluoride
0135-0527	Sensodyne	potassium nitrate and sodium fluoride
0135-0528	Sensodyne	potassium nitrate and sodium fluoride
0135-0450	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0460	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0480	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0481	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0484	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0486	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0492	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride
0135-0520	SENSODYNE PRONAMEL	potassium nitrate and sodium fluoride