Home NDC 41250-576 Oral Antivavity
Product NDC 41250-576
11-digit product format 412500576
Labeler code 41250
Product ID 41250-576_4b33fb12-ad0a-8dd2-e063-6294a90a032b
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form MOUTHWASH
Route ORAL
Labeler Meijer, Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-02-06
Substance SODIUM FLUORIDE
Active strength .1 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 Oral Antivavity
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .1 mg/mL
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 313029 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-576-86 Oral Antivavity 1000 mL in 1 BOTTLE, PLASTIC MOUTHWASH 1000 13
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 CETYLPYRIDINIUM CHLORIDE INACTIVE INGREDIENT D9OM4SK49P ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 PHOSPHORIC ACID INACTIVE INGREDIENT E4GA8884NN ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 POLOXAMER 407 INACTIVE INGREDIENT TUF2IVW3M2 ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT 22ADO53M6F ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-576 ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC] 12 Current NDC, Legacy NDC, 1 package rows 20250423_af34f83f-1328-4897-9d04-72ca5a4101bf.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 39 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 41250-576-86 41250057686 1000 mL in 1 BOTTLE, PLASTIC (41250-576-86) 1000 ml 2015-02-06 0000-00-00 No No Current