Home NDC 53045-300 Frenna AC
Product NDC 53045-300
11-digit product format 530450300
Labeler code 53045
Product ID 53045-300_6b95574e-24cf-4cb9-a23a-284c2981fa33
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Aluminum Chloride
Dosage form SOLUTION
Route DENTAL; ORAL; TOPICAL
Labeler Dharma Research, inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2013-01-01
Substance ALUMINUM CHLORIDE
Active strength 8.75 g/35g
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 Code Status Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 53045-300-30 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 53045-300-30 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base Frenna AC
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLORIDE 8.75 g/35g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3CYT62D3GA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 244613 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53045-300-30 Frenna AC 35 g in 1 BOTTLE, PLASTIC SOLUTION 35 2
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53045-300 FRENNA AC (ALUMINUM CHLORIDE) SOLUTION [DHARMA RESEARCH, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20201107_d09ae142-6fd5-45e4-a9c4-44428885ccaf.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 1 of 1 · 1 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 53045-300-30 53045030030 35 g in 1 BOTTLE, PLASTIC (53045-300-30) 35 g 2013-01-01 0000-00-00 No No Current