Home NDC 85751-001 DRY GRIP
Product NDC 85751-001
11-digit product format 857510001
Labeler code 85751
Product ID 85751-001_36a79c9d-27bd-78f3-e063-6394a90a2da6
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chloride
Dosage form SPRAY, METERED
Route TOPICAL
Labeler Chongqing Alefa Technology Co., Ltd.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-03
Substance ALUMINUM CHLORIDE
Active strength 15 g/100g
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 DRY GRIP
Listing expiration 2026-12-31 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 85751-001-01 DRY GRIP 60 g in 1 BOTTLE, SPRAY SPRAY, METERED 60 1 85751-001-01 DRY GRIP 1 in 1 BOX SPRAY, METERED 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 Marketing start Sample Exclude flag Status 85751-001-01 85751000101 1 BOTTLE, SPRAY in 1 BOX (85751-001-01) / 60 g in 1 BOTTLE, SPRAY 2025-06-04 No No Current