Home NDC 70108-076 Crayola ANTICAVITY BUBBLE GUM FLAVOR
Product NDC 70108-076
11-digit product format 701080076
Labeler code 70108
Product ID 70108-076_10fef64a-932f-4ef2-8eca-563a4f2d2b3f
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Ashtel Studios, Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-06
Marketing end 2028-03-31
Substance SODIUM FLUORIDE
Active strength .243 g/100g
NDC exclude flag No
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 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 70108-076-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 70108-076-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 70108-076-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 70108-076-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 70108-076-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70108-076-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70108-076-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Crayola ANTICAVITY BUBBLE GUM FLAVOR Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .243 g/100g
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70108-076-01 Crayola ANTICAVITY BUBBLE GUM FLAVOR 113 g in 1 TUBE PASTE, DENTIFRICE 113 2 70108-076-01 Crayola ANTICAVITY BUBBLE GUM FLAVOR 1 in 1 BOX PASTE, DENTIFRICE 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70108-076 CRAYOLA ANTICAVITY BUBBLE GUM FLAVOR (SODIUM FLUORIDE) PASTE, DENTIFRICE [ASHTEL STUDIOS, INC.] 2 Current NDC, 2 package rows 20250323_ec66246f-06e2-4da1-b9d5-ce2a7815ffd1.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 29 of 50 · 995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Supersmile Professional Whitening TP Citrus Blast SODIUM MONOFLUOROPHOSPHATE Robell Research, Inc 25039552-c35d-a69d-e063-6394a90ab103 2026-01-08 Warnings Exact identifier application number: M021 Supersmile Professional Whitening TP Citrus Blast SODIUM MONOFLUOROPHOSPHATE Robell Research, Inc 2504686d-b053-51d0-e063-6394a90a789f 2026-01-08 Warnings Exact identifier application number: M021 Supersmile Professional Whitening TP Peppy Mint 8 oz SODIUM MONOFLUOROPHOSPHATE Robell Research, Inc 25121ebb-922b-719d-e063-6394a90a23d3 2026-01-08 Warnings Exact identifier application number: M021 Crest Pro-health Gum Detoxify Deep Clean STANNOUS FLUORIDE The Procter & Gamble Manufacturing Company f498b727-c38c-1d67-e053-2995a90a0f11 2026-01-08 Warnings Exact identifier application number: M021 DG health Sensitive Maximum Strength POTASSIUM NITRATE, SODIUM FLUORIDE Dolgencorp, LLC 81cd5d37-3751-625f-e053-2a91aa0a6dfd 2026-01-08 Warnings Exact identifier application number: M021 Crest 3D White Advanced Glamorous White SODIUM FLUORIDE The Procter & Gamble Manufacturing Company f5b18988-68c7-40f9-e053-2995a90a22bc 2026-01-08 Warnings Exact identifier application number: M021 CVS Restore and Defend Sensitive Whitening STANNOUS FLUORIDE CVS Pharmacy 81b72da2-7f41-74ca-e053-2a91aa0a9646 2026-01-08 Warnings Exact identifier application number: M021 Gum and Enamel Repair STANNOUS FLUORIDE CVS ccad05d4-7f05-bebd-e053-2a95a90aa52c 2026-01-08 Warnings Exact identifier application number: M021 CVS Pharmacy Pro Defense FLUORIDE CVS Pharmacy 445ec57e-dc3c-49a0-8ca9-4806fcdc0303 2026-01-08 Warnings Exact identifier application number: M021 Gum Detoxify STANNOUS FLUORIDE Walmart ad3f645d-aaf9-2800-e053-2a95a90ab62f 2026-01-08 Warnings Exact identifier application number: M021 CVS Complete Protection STANNOUS FLOURIDE CVS b681b5e4-a0e1-8d0f-e053-2a95a90aa672 2026-01-06 Warnings Exact identifier application number: M021 Complete Protection STANNOUS FLUORIDE Target 03708e08-0189-b83d-e063-6394a90a50e6 2026-01-06 Warnings Exact identifier application number: M021 Brush Buddies Mouthwash 12oz Star Wars Saber Strike Strawberry SODIUM FLUORIDE Kingkey MBC Life Technology Group co., LTD. 4998c0e6-1de3-11cd-e063-6294a90acb6f 2026-01-01 Warnings Exact identifier application number: M021 Exceed Total Care Sensitive Spearmint Tooth Polish POTASSIUM NITRATE AND SODIUM FLUORIDE Melaleuca, Inc dc620d3f-880f-df05-e053-2995a90a8409 2025-12-31 Warnings Exact identifier application number: M021 Exceed Total Care Sensitive Peppermint Tooth Polish POTASSIUM NITRATE AND SODIUM FLUORIDE Melaleuca, Inc ed2179a4-3d19-6481-e053-2995a90ad655 2025-12-31 Warnings Exact identifier application number: M021 Koala Pals Berrylicious SODIUM FLUORIDE Melaleuca, Inc. 6624be86-c9a8-53b8-e053-2a91aa0a87ef 2025-12-31 Warnings Exact identifier application number: M021 Whitening Tooth Polish SODIUM FLUORIDE Melaleuca, Inc. 6893405a-a2c4-068e-e053-2a91aa0ae5b1 2025-12-31 Warnings Exact identifier application number: M021 Gel 1100 Mint SODIUM FLUORIDE Dental Alliance Holdings LLC f125fb04-5045-5367-e053-2a95a90aa73b 2025-12-29 Warnings Exact identifier application number: M021 Gracie Square Hospital Amenity SODIUM MONOFLUOROPHOSPHATE ASP Global, LLc 89d81053-6950-465e-a5b1-cbf841d7afcb 2025-12-29 Warnings Exact identifier application number: M021 CloSYS Fluoride Rinse SODIUM FLUORIDE Rowpar Pharmaceuticals, Inc. 1a994f24-99ee-4b27-aab0-e816931a22c8 2025-12-23 Warnings Exact identifier application number: M021
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 70108-076-01 70108007601 1 TUBE in 1 BOX (70108-076-01) / 113 g in 1 TUBE 1 tube 2023-09-06 2028-03-31 No No Historical