Home NDC 85816-1025 BM Alum (Kali Alum Sulph)
Product NDC 85816-1025
11-digit product format 858161025
Labeler code 85816
Product ID 85816-1025_38017047-1da3-e0c0-e063-6394a90aec91
Type HUMAN OTC DRUG
Nonproprietary name Alum
Dosage form TABLET
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-01
Substance POTASSIUM ALUM
Active strength 6 [hp_X]/60mg
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings and Storage: Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
Additional Listing Data#
Finished product Yes
Brand name base BM Alum (Kali Alum Sulph)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM ALUM 6 [hp_X]/60mg
Harmonized Identifiers# Field, Values table Field Values Unii 1L24V9R23S
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-1025-1 BM Alum (Kali Alum Sulph) 30000 mg in 1 BOTTLE, GLASS TABLET 30000 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85816-1025-1 85816102501 30000 mg in 1 BOTTLE, GLASS (85816-1025-1) 30000 mg 2025-06-01 No No Current