Manufacturing Establishments1
FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.
BM Private Limited
BM Private Limited
645599762
Products1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
BM Potassium dichromate (Kali Dichrom)
Product Details
Drug Labeling Information
Complete FDA-approved labeling information including indications, dosage, warnings, contraindications, and other essential prescribing details.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Entire
package
INDICATIONS & USAGE SECTION
Uses
See the leaflet enclosed for detail.
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.
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.
OTC - ACTIVE INGREDIENT SECTION
Potassium Dichromate
OTC - PURPOSE SECTION
Uses
See the leaflet enclosed for detail.
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.
INACTIVE INGREDIENT SECTION
Inactive ingredients: Lactose; MAGNESIUM STEARATE