BM NAT SULPH- natrum sulphuricum tablet

BM Nat Sulph by

Drug Labeling and Warnings

BM Nat Sulph by is a Homeopathic medication manufactured, distributed, or labeled by BM Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Natrum Sulphuricum

INACTIVE INGREDIENT

Inactive Ingredients: Lactose, Magnesium Stearate

INDICATIONS & USAGE

Uses
See the leaflet enclosed for detail.

PURPOSE

Uses
See the leaflet enclosed for detail.

DOSAGE & ADMINISTRATION

Directions:
Adult: Four tablets three times a day.
Ages below 12: half of the same or as prescribed by a homeopathic physician.

CONTRAINDICATIONS

Contra-indications:
Traditional biochemic remedy do not interact with other remedies, herbs, or other supplements.

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.

KEEP OUT OF REACH OF CHILDREN

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.

PRINCIPAL DISPLAY PANEL

Package 1 (30g)

Package 2 (500g)

INGREDIENTS AND APPEARANCE

BM NAT SULPH 
natrum sulphuricum tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85816-1011
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM SULFATE	6 [hp_X]  in 60 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)	58.6 mg  in 60 mg
MAGNESIUM STEARATE (UNII: 70097M6I30)	1.25 mg  in 60 mg

Product Characteristics
Color	white (White Dissolvable Tablets)	Score	no score
Shape	ROUND (Round Dissolvable Tablets)	Size	90mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85816-1011-1	30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/2015
2	NDC: 85816-1011-2	500000 mg in 1 JAR; Type 0: Not a Combination Product	01/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/2015

Labeler - BM Private Limited (645599762)

Establishment
Name	Address	ID/FEI	Business Operations
BM Private Limited		645599762	manufacture(85816-1011) , pack(85816-1011) , label(85816-1011)