Home NDC 76670-0012 Double X CONCENTRATED
Product NDC 76670-0012
11-digit product format 766700012
Labeler code 76670
Product ID 76670-0012_2c487d0a-fb67-49ad-e063-6294a90a939b
Type HUMAN OTC DRUG
Nonproprietary name Cetylpyridinium Chloride
Dosage form MOUTHWASH
Route ORAL
Labeler DOCSMEDI Co., Ltd.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-02
Substance CETYLPYRIDINIUM CHLORIDE
Active strength 2.3 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76670-0012-2 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76670-0012-2 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 Double X CONCENTRATED
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CETYLPYRIDINIUM CHLORIDE 2.3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination D9OM4SK49P Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2590919 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76670-0012-1 Double X CONCENTRATED 30 mL in 1 CONTAINER MOUTHWASH 30 5 76670-0012-2 Double X CONCENTRATED 2 in 1 CARTON MOUTHWASH 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76670-0012 DOUBLE X CONCENTRATED (CETYLPYRIDINIUM CHLORIDE) MOUTHWASH [DOCSMEDI CO., LTD.] 5 Current NDC, Legacy NDC, 2 package rows 20250123_411be334-364c-4074-8d0b-8dda332f87de.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 6 of 49 · 974 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 76670-0012-1 76670001201 30 mL in 1 CONTAINER 30 ml Historical 76670-0012-2 76670001202 2 CONTAINER in 1 CARTON (76670-0012-2) / 30 mL in 1 CONTAINER (76670-0012-1) 2 container 2022-01-02 0000-00-00 No No Current