SUBSIDIUM- naja naja strip

Subsidium by

Drug Labeling and Warnings

Subsidium by is a Homeopathic medication manufactured, distributed, or labeled by Subsidium, LLC, Coral Pharmaceuticals, Ldt. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

For oral use only

If symptoms persist stop using this product and consult a physician

Side effects may include headache, nausea, sore throat

Directions for use

Dissolve one (1) strip under the tongue daily. It may take up to 15 doses to start relief.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

ACTIVE INGREDIENT

Naja Naja H 10X

INACTIVE INGREDIENT

Carboxymethyelcellulose, sodium chloride 0.9%, water, natural orange flavorings, sucrose , thimerosol

PURPOSE

Immune Modulator

PREGNANCY OR BREAST FEEDING

Not for use by pregnant or nursing women

Uses

Temporarily reduces joint inflammation and pain and general associated pain.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUBSIDIUM 
naja naja strip

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70052-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	10 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)
THIMEROSAL (UNII: 2225PI3MOV)
ORANGE OIL (UNII: AKN3KSD11B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70052-001-01	15 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/01/2015

Labeler - Subsidium, LLC (079865137)

Registrant - Subsidium, LLC (079865137)

Establishment
Name	Address	ID/FEI	Business Operations
Coral Pharmaceuticals, Ldt		815177490	manufacture(70052-001)