Home NDC 85751-002 PURE DRY
Product NDC 85751-002
11-digit product format 857510002
Labeler code 85751
Product ID 85751-002_500d4d13-2714-5b76-e063-6294a90ac763
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Chongqing Alefa Technology Co., Ltd.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-22
Substance ALUMINUM CHLORIDE
Active strength 15 g/100g
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 PURE DRY
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLORIDE 15 g/100g
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 85751-002-01 PURE DRY 60 g in 1 BOTTLE LIQUID 60 1 85751-002-02 PURE DRY 1 in 1 BOX LIQUID 1 1
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 Sample Exclude flag Status 85751-002-01 85751000201 60 g in 1 BOTTLE 60 g Historical 85751-002-02 85751000202 1 BOTTLE in 1 BOX (85751-002-02) / 60 g in 1 BOTTLE (85751-002-01) 1 bottle 2026-04-22 No No Current