native whitening

Generic: sodium fluoride

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

Drug Facts

Product Profile

Brand Name native whitening
Generic Name sodium fluoride
Labeler procter & gamble manufacturing company
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium fluoride 1.4 mg/g

Manufacturer
Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-973
Product ID 37000-973_47e32c0d-afe6-af72-e063-6394a90af9cf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2020-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000973
Hyphenated Format 37000-973

Supplemental Identifiers

RxCUI
891775
UNII
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 native whitening (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 1.4 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (37000-973-41) / 116 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (1.4 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "47e32c0d-afe6-af72-e063-6394a90af9cf", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["891775"], "spl_set_id": ["a5248d35-f488-3457-e053-2995a90a411e"], "manufacturer_name": ["Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (37000-973-41)  / 116 g in 1 TUBE", "package_ndc": "37000-973-41", "marketing_start_date": "20200101"}], "brand_name": "Native Whitening", "product_id": "37000-973_47e32c0d-afe6-af72-e063-6394a90af9cf", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "37000-973", "generic_name": "Sodium Fluoride", "labeler_name": "Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Native", "brand_name_suffix": "Whitening", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1.4 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200101", "listing_expiration_date": "20271231"}