Home NDC 41520-415 Care One
Product NDC 41520-415
11-digit product format 415200415
Labeler code 41520
Product ID 41520-415_47e54e5e-4bd7-00ce-e063-6394a90a99e8
Type HUMAN OTC DRUG
Nonproprietary name Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler American Sales
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-01-20
Substance SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength .15; 5 g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 41520-415-09 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 41520-415-09 e2bbac7714bc…27bdfed8d636…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Care One
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .15 g/100g POTASSIUM NITRATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup RU45X2JN0Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038929 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41520-415-02 Care OneMaximum Strength 113 g in 1 TUBE PASTE, DENTIFRICE 113 6 41520-415-09 Care OneMaximum Strength 1 in 1 CARTON PASTE, DENTIFRICE 1 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POTASSIUM NITRATE ACTIVE INGREDIENT RU45X2JN0Z CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 NITRATE ION ACTIVE MOIETY T93E9Y2844 CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 SODIUM PHOSPHATE, TRIBASIC INACTIVE INGREDIENT A752Q30A6X CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41520-415 CARE ONE MAXIMUM STRENGTH (FLUORIDE) PASTE, DENTIFRICE [AMERICAN SALES] 5 Current NDC, Legacy NDC, 2 package rows 20250119_1b6618ea-6533-41d7-be2c-13bb9e108dc5.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 19 of 40 · 786 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Povi-One POVIDONE-IODINE 10% TOPICAL Elevate Oral Care f5252b4f-5e14-509e-e053-2995a90a6db8 2025-09-18 Warnings Exact identifier application number: M022 Patterson Dental Topical Anesthetic BENZOCAINE Patterson Dental 3f199947-bf25-914b-e063-6394a90a8a6f 2025-09-18 Warnings Exact identifier application number: M022 Patterson Dental Topical Anesthetic BENZOCAINE Patterson Dental 3f199947-bf28-914b-e063-6394a90a8a6f 2025-09-18 Warnings Exact identifier application number: M022 Patterson Dental Topical Anesthetic BENZOCAINE Patterson Dental 3f19a1a7-c234-8d26-e063-6394a90ad7e9 2025-09-18 Warnings Exact identifier application number: M022 McKesson Orasol Gel BENZOCAINE 20% McKesson Medical-Surgical cc8724f4-c482-5e7d-e053-2a95a90a608f 2025-09-09 Warnings Exact identifier application number: M022 MGC Health Drops Sugar Free Lemon Mint MENTHOL Medical Group Care LLC 3d70bca7-e830-e693-e063-6294a90a73f9 2025-08-28 Warnings Exact identifier application number: M022 Exchange Select Drops Sugar Free Lemon Mint MENTHOL Army & Air Force Exchange Service 3d70450f-04ea-1885-e063-6294a90a05bd 2025-08-28 Warnings Exact identifier application number: M022 Ki No Sin CALCIUM CARBONATE NPG Bio Pharmaceuticals Co.,Ltd. 21fa2bad-5b8b-8aac-e063-6394a90a9f49 2025-08-27 Warnings Exact identifier application number: M022 R Cos CALCIUM CARBONATE NPG Bio Pharmaceuticals Co.,Ltd. 21fa767a-1344-5ed9-e063-6394a90a5fe6 2025-08-27 Warnings Exact identifier application number: M022 Na Mi Cal CALCIUM CARBONATE NPG Bio Pharmaceuticals Co.,Ltd. 20cfbcd1-eb13-933c-e063-6294a90a7e59 2025-08-27 Warnings Exact identifier application number: M022 Ki No Sin CALCIUM CARBONATE NPG Bio Pharmaceuticals Co.,Ltd. 20cf8f80-c638-4d94-e063-6294a90a5400 2025-08-27 Warnings Exact identifier application number: M022 Charm Tex FLUORIDE SODIUM MONOFLUOROPHOSPHATE Yangzhou Hongshengding Chemical Co.,Ltd. 63a69664-8611-4d69-b871-8d1d5b553e5c 2025-08-18 Warnings Exact identifier application number: M022 QUALITY CHOICE SALINE SODIUM CHLORIDE QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) f51491d8-12ad-4b1b-a171-c621bfdcc341 2025-08-12 Warnings Exact identifier application number: M022 MGC Health Drops Sugar Free Lemon Mint MENTHOL Xiamen Kang Zhongyuan Biotechnology Co., Ltd. b9227966-847c-40c3-87f2-8bea3954ec84 2025-08-12 Warnings Exact identifier application number: M022 Exchange Select Drops Sugar Free Lemon Mint MENTHOL Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 5f4b1960-43ac-4c74-9410-210c48bd8a1b 2025-08-12 Warnings Exact identifier application number: M022 HurriCaine Topical Anesthetic BENZOCAINE Beutlich Pharmaceuticals, LLC 113cdb83-0fdd-40f2-8ee6-b771dca99713 2025-08-12 Warnings Exact identifier application number: M022 CVS Pharmacy Maximum Strength BENZOCAINE CVS Pharmacy 13bf31c1-78e3-459f-9249-b0b6e2c17a13 2025-08-12 Warnings Exact identifier application number: M022 Rexall Maximum Strength BENZOCAINE Rexall 8f6e2780-cfb7-4bef-9b7d-13cb80d8923e 2025-08-12 Warnings Exact identifier application number: M022 Walgreens Maximum Strength BENZOCAINE Walgreens 8f24309d-d393-455a-a9a5-a55344adf36b 2025-08-12 Warnings Exact identifier application number: M022 Oral Anesthetic Liquid BENZOCAINE Meijer, Inc. 0321c480-e150-421d-e063-6294a90ad687 2025-08-12 Warnings Exact identifier application number: M022
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 41520-415-02 41520041502 113 g in 1 TUBE 113 g Historical 41520-415-09 41520041509 1 TUBE in 1 CARTON (41520-415-09) / 113 g in 1 TUBE (41520-415-02) 1 tube 2012-11-15 0000-00-00 No No Current