Home NDC 58933-049 Kids Crest Cavity Protection
Product NDC 58933-049
11-digit product format 589330049
Labeler code 58933
Product ID 58933-049_53bfcf0e-1d39-5488-e063-6294a90a9307
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Procter & Gamble Manufactura, S. de R.L. de C.V.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2002-09-05
Substance SODIUM FLUORIDE
Active strength 1.5 mg/g
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Kids Crest Cavity Protection
Brand name suffix Sparkle Fun
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 891775 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58933-049-01 Kids Crest Cavity ProtectionSparkle Fun 24 g in 1 TUBE PASTE, DENTIFRICE 24 10 58933-049-06 Kids Crest Cavity ProtectionSparkle Fun 170 g in 1 TUBE PASTE, DENTIFRICE 170 10 58933-049-13 Kids Crest Cavity ProtectionSparkle Fun 3 in 1 CELLO PACK PASTE, DENTIFRICE 3 10 58933-049-13 Kids Crest Cavity ProtectionSparkle Fun 130 g in 1 TUBE PASTE, DENTIFRICE 130 10 58933-049-22 Kids Crest Cavity ProtectionSparkle Fun 62 g in 1 TUBE PASTE, DENTIFRICE 62 10 58933-049-22 Kids Crest Cavity ProtectionSparkle Fun 1 in 1 CARTON PASTE, DENTIFRICE 1 10 58933-049-46 Kids Crest Cavity ProtectionSparkle Fun 1 in 1 CARTON PASTE, DENTIFRICE 1 10 58933-049-46 Kids Crest Cavity ProtectionSparkle Fun 130 g in 1 TUBE PASTE, DENTIFRICE 130 10 58933-049-62 Kids Crest Cavity ProtectionSparkle Fun 62 g in 1 TUBE PASTE, DENTIFRICE 62 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58933-049 KIDS CREST CAVITY PROTECTION SPARKLE FUN (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURA, S. DE R.L. DE C.V.] 7 Current NDC, Legacy NDC, 9 package rows 20240207_df182c22-bbf1-448d-81e8-35cb431d2afc.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 5 of 50 · 995 matching rows.
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 58933-049-01 58933004901 24 g in 1 TUBE (58933-049-01) 24 g 2002-09-05 0000-00-00 No No Current 58933-049-06 58933004906 170 g in 1 TUBE 170 g Historical 58933-049-13 58933004913 3 TUBE in 1 CELLO PACK (58933-049-13) / 130 g in 1 TUBE 3 tube 2020-11-01 No No Current 58933-049-22 58933004922 1 TUBE in 1 CARTON (58933-049-22) / 62 g in 1 TUBE 1 tube 2020-11-01 0000-00-00 No No Current 58933-049-46 58933004946 1 TUBE in 1 CARTON (58933-049-46) / 130 g in 1 TUBE 1 tube 2020-11-01 No No Current 58933-049-62 58933004962 62 g in 1 TUBE 62 g Historical 58933-049-85 58933004985 1 TUBE in 1 CARTON (58933-049-85) / 24 g in 1 TUBE 1 tube 2002-09-05 No No Current