crest cavity protection regular
Generic: sodium fluoride
Labeler: the procter & gamble manufacturing companyDrug Facts
Product Profile
Brand Name
crest cavity protection regular
Generic Name
sodium fluoride
Labeler
the procter & gamble manufacturing company
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium fluoride 1.5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
37000-005
Product ID
37000-005_47e4b9fd-1f5a-451e-e063-6394a90af1c2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
1984-08-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37000005
Hyphenated Format
37000-005
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 cavity protection regular (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.5 mg/g
Packaging
- 1 TUBE in 1 CARTON (37000-005-05) / 232 g in 1 TUBE
- 1 TUBE in 1 CARTON (37000-005-10) / 24 g in 1 TUBE (37000-005-08)
- 2 TUBE in 1 CARTON (37000-005-11) / 161 g in 1 TUBE
- 1 TUBE in 1 CARTON (37000-005-24) / 68 g in 1 TUBE
- 1 TUBE in 1 CARTON (37000-005-42) / 119 g in 1 TUBE
- 1 TUBE in 1 CARTON (37000-005-57) / 161 g in 1 TUBE
- 3 CARTON in 1 CELLO PACK (37000-005-90) / 1 TUBE in 1 CARTON / 161 g in 1 TUBE
Packages (7)
37000-005-05
1 TUBE in 1 CARTON (37000-005-05) / 232 g in 1 TUBE
37000-005-10
1 TUBE in 1 CARTON (37000-005-10) / 24 g in 1 TUBE (37000-005-08)
37000-005-11
2 TUBE in 1 CARTON (37000-005-11) / 161 g in 1 TUBE
37000-005-24
1 TUBE in 1 CARTON (37000-005-24) / 68 g in 1 TUBE
37000-005-42
1 TUBE in 1 CARTON (37000-005-42) / 119 g in 1 TUBE
37000-005-57
1 TUBE in 1 CARTON (37000-005-57) / 161 g in 1 TUBE
37000-005-90
3 CARTON in 1 CELLO PACK (37000-005-90) / 1 TUBE in 1 CARTON / 161 g in 1 TUBE
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "47e4b9fd-1f5a-451e-e063-6394a90af1c2", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["891775"], "spl_set_id": ["6caf3f2e-70a2-4530-99fa-f5af7e4c511a"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (37000-005-05) / 232 g in 1 TUBE", "package_ndc": "37000-005-05", "marketing_start_date": "19840802"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37000-005-10) / 24 g in 1 TUBE (37000-005-08)", "package_ndc": "37000-005-10", "marketing_start_date": "19840802"}, {"sample": false, "description": "2 TUBE in 1 CARTON (37000-005-11) / 161 g in 1 TUBE", "package_ndc": "37000-005-11", "marketing_start_date": "20190910"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37000-005-24) / 68 g in 1 TUBE", "package_ndc": "37000-005-24", "marketing_start_date": "20190910"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37000-005-42) / 119 g in 1 TUBE", "package_ndc": "37000-005-42", "marketing_start_date": "20190910"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37000-005-57) / 161 g in 1 TUBE", "package_ndc": "37000-005-57", "marketing_start_date": "20190910"}, {"sample": false, "description": "3 CARTON in 1 CELLO PACK (37000-005-90) / 1 TUBE in 1 CARTON / 161 g in 1 TUBE", "package_ndc": "37000-005-90", "marketing_start_date": "20190910"}], "brand_name": "Crest Cavity Protection Regular", "product_id": "37000-005_47e4b9fd-1f5a-451e-e063-6394a90af1c2", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "37000-005", "generic_name": "Sodium Fluoride", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Crest Cavity Protection Regular", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1.5 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19840802", "listing_expiration_date": "20271231"}