spry dentifrice

Generic: toothpaste

Labeler: xlear inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name spry dentifrice
Generic Name toothpaste
Labeler xlear inc.
Dosage Form PASTE, DENTIFRICE
Routes
ORAL
Active Ingredients

sodium fluoride 2.43 mg/g

Manufacturer
Xlear Inc.

Identifiers & Regulatory

Product NDC 27017-142
Product ID 27017-142_43567bbc-b07f-b605-e063-6294a90aad78
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2017-06-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27017142
Hyphenated Format 27017-142

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 spry dentifrice (source: ndc)
Generic Name toothpaste (source: ndc)
Application Number M021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.43 mg/g
source: ndc
Packaging
  • 1 g in 1 TUBE (27017-142-01)
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (2.43 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43567bbc-b07f-b605-e063-6294a90aad78", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["891775"], "spl_set_id": ["43567bbc-b07e-b605-e063-6294a90aad78"], "manufacturer_name": ["Xlear Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 TUBE (27017-142-01)", "package_ndc": "27017-142-01", "marketing_start_date": "20170611"}], "brand_name": "Spry Dentifrice", "product_id": "27017-142_43567bbc-b07f-b605-e063-6294a90aad78", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "27017-142", "generic_name": "Toothpaste", "labeler_name": "Xlear Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Spry Dentifrice", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "2.43 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170611", "listing_expiration_date": "20261231"}