BM Alum (Kali Alum Sulph)
BM Alum (Kali Alum Sulph)
38017047-1da2-e0c0-e063-6394a90aec91
HUMAN OTC DRUG LABEL
Jun 20, 2025
BM Private Limited
DUNS: 645599762
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Alum
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
Product Classification
Product Specifications
INGREDIENTS (3)
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Entire package label
INDICATIONS & USAGE SECTION
Uses
See the leaflet enclosed for detail.
CONTRAINDICATIONS SECTION
Contra-indications:
Traditional biochemic remedy do not interact with other remedies, herbs, or
other supplements.
WARNINGS SECTION
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.
DOSAGE & ADMINISTRATION SECTION
Directions:
Adult: Four tablets three times a day.
Ages below 12: half of the same or as prescribed by a homeopathic physician.
INACTIVE INGREDIENT SECTION
Inactive ingredients: Lactose; MAGNESIUM STEARATE
OTC - ACTIVE INGREDIENT SECTION
Alum
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
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.
OTC - PURPOSE SECTION
Uses
See the leaflet enclosed for detail.