Home NDC 69693-715 CERTAIN DRI
Product NDC 69693-715
11-digit product format 696930715
Labeler code 69693
Product ID 69693-715_46a906ee-127a-793d-e063-6394a90a1140
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Clarion Brands, LLC
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance ALUMINUM CHLORIDE
Active strength .12 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 CERTAIN DRI
Brand name suffix ROLL-ON
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLORIDE .12 mg/mL
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 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 69693-715-01 CERTAIN DRIROLL-ON 1 in 1 POUCH LIQUID 1 7 69693-715-01 CERTAIN DRIROLL-ON 1.3 mL in 1 APPLICATOR LIQUID 1.3 7 69693-715-12 CERTAIN DRIROLL-ON 35.5 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 35.5 7 69693-715-12 CERTAIN DRIROLL-ON 1 in 1 CARTON LIQUID 1 7 69693-715-20 CERTAIN DRIROLL-ON 2 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 2 7 69693-715-20 CERTAIN DRIROLL-ON 1 in 1 CARTON LIQUID 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69693-715 CERTAIN DRI ROLL-ON (ALUMINUM CHLORIDE) LIQUID [CLARION BRANDS, LLC] 6 Current NDC, Legacy NDC, 6 package rows 20241225_24282949-5c38-d3fb-adbe-f5c699f87d73.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 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69693-715-01 69693071501 1 APPLICATOR in 1 POUCH (69693-715-01) / 1.3 mL in 1 APPLICATOR 1 applicator 2016-04-01 0000-00-00 No No Current 69693-715-12 69693071512 1 BOTTLE, WITH APPLICATOR in 1 CARTON (69693-715-12) / 35.5 mL in 1 BOTTLE, WITH APPLICATOR 2015-11-01 0000-00-00 No No Current 69693-715-20 69693071520 1 BOTTLE, WITH APPLICATOR in 1 CARTON (69693-715-20) / 2 mL in 1 BOTTLE, WITH APPLICATOR 2015-11-01 0000-00-00 No No Current