Home NDC 0273-0241-22 Oral B NeutraCare
Product NDC 0273-0241
Requested package NDC 0273-0241-22
11-digit product format 002730241
Labeler code 0273
Product ID 0273-0241_f16222d2-3664-bd47-e053-2995a90abfed
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Sodium Fluoride
Dosage form SOLUTION
Route ORAL
Labeler YOUNG DENTAL MANUFACTURING CO 1, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2014-11-23
Marketing end 0000-00-00
Substance SODIUM FLUORIDE
Active strength 1 mg/g
NDC exclude flag No
Listing certified through 2024-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0273-0241-22 Oral B NeutraCare Mint Menthe 57 g in 1 TUBE SOLUTION 57 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Sodium Fluoride ACTIVE INGREDIENT 8ZYQ1474W7 ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 FLUORIDE ION ACTIVE MOIETY Q80VPU408O ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 phosphoric acid INACTIVE INGREDIENT E4GA8884NN ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 spearmint oil INACTIVE INGREDIENT C3M81465G5 ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 sucralose INACTIVE INGREDIENT 96K6UQ3ZD4 ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2 Water INACTIVE INGREDIENT 059QF0KO0R ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0273-0241 ORAL B NEUTRACARE MINT MENTHE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC] 5 Legacy NDC, 1 package rows 20230105_8605e7a1-9aa5-476d-8730-1cd663736c73.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0273-0241-22 00273024122 57 g in 1 TUBE (0273-0241-22) 57 g 2014-11-23 0000-00-00 No No Current