crest premium plus sensitivity active foam

Generic: sodium fluoride and potassium nitrate

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name crest premium plus sensitivity active foam
Generic Name sodium fluoride and potassium nitrate
Labeler the procter & gamble manufacturing company
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

potassium nitrate 50 mg/g, sodium fluoride 1.4 mg/g

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-995
Product ID 37000-995_47e4e251-448a-efc5-e063-6294a90a56a8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2021-01-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000995
Hyphenated Format 37000-995

Supplemental Identifiers

RxCUI
1038800
UNII
RU45X2JN0Z 8ZYQ1474W7

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name crest premium plus sensitivity active foam (source: ndc)
Generic Name sodium fluoride and potassium nitrate (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
  • 1.4 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (37000-995-52) / 147 g in 1 TUBE
  • 1 TUBE in 1 CARTON (37000-995-70) / 198 g in 1 TUBE
source: ndc

Packages (2)

37000-995-52 1 TUBE in 1 CARTON (37000-995-52) / 147 g in 1 TUBE 37000-995-70 1 TUBE in 1 CARTON (37000-995-70) / 198 g in 1 TUBE

Ingredients (2)

potassium nitrate (50 mg/g) sodium fluoride (1.4 mg/g)

Linked Drug Pages (1)

Crest Premium Plus Sensitivity Active Foam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "47e4e251-448a-efc5-e063-6294a90a56a8", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038800"], "spl_set_id": ["b8535d1c-cf15-f353-e053-2a95a90a7974"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (37000-995-52)  / 147 g in 1 TUBE", "package_ndc": "37000-995-52", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37000-995-70)  / 198 g in 1 TUBE", "package_ndc": "37000-995-70", "marketing_start_date": "20210107"}], "brand_name": "Crest Premium Plus Sensitivity Active Foam", "product_id": "37000-995_47e4e251-448a-efc5-e063-6294a90a56a8", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "37000-995", "generic_name": "Sodium Fluoride and Potassium Nitrate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Crest Premium Plus", "brand_name_suffix": "Sensitivity Active Foam", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.4 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210107", "listing_expiration_date": "20271231"}