Home NDC 41167-0937 ACT Anticavity Fluoride Arctic Blast
Product NDC 41167-0937
11-digit product format 411670937
Labeler code 41167
Product ID 41167-0937_36e783b7-17fc-4f04-a208-8b5f673041a9
Type HUMAN OTC DRUG
Nonproprietary name sodium fluoride
Dosage form MOUTHWASH
Route TOPICAL
Labeler Chattem, Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-01-02
Substance SODIUM FLUORIDE
Active strength .2 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 ACT Anticavity Fluoride Arctic Blast
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .2 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 240698 Internal RxNorm lookup 656809 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 41167-0937-2 ACT Anticavity Fluoride Arctic Blast 532 mL in 1 BOTTLE, PLASTIC MOUTHWASH 532 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41167-0937 ACT ANTICAVITY FLUORIDE ARCTIC BLAST (SODIUM FLUORIDE) MOUTHWASH [CHATTEM, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20250206_2d5c1ce7-3c3e-415e-9469-a8d3ddfe2c57.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 41167-0937-2 41167093702 532 mL in 1 BOTTLE, PLASTIC (41167-0937-2) 532 ml 2019-01-02 0000-00-00 No No Current