ACTIVE INGREDIENT:

Arnica Montana 30X.

PURPOSE:

Anti-Inflammatory

WARNINGS:

If pregnant or breast-feeding ask a health professional before use. Discontinue use if any adverse reactions occur. Contact your physician, if symptoms do not subside within 14 days.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if seal is broken or shows any signs of tampering.

KEEP OUT OF REACH OF CHILDREN:

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults, three tablets, three times a day. Not intended for children under 12 years of age. This product is a sublingual application.

USES:

Temporary relief of bruising, swelling and pain associated with soft tissue injury.

INACTIVE INGREDIENTS:

Copovidone, Crospovidone, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose, Silicon Dioxide, and Sorbitol.

QUESTIONS:

Formulated and Distributed

by VitaMedica Corp.

Torrance, CA 90502

888-367-8605 VitaMedica.com

NDC 65111-005-66

PACKAGE DISPLAY LABEL

VitaMedica

Arnica Montana

30X HPUS

REDUCES

Bruising, Swelling & Pain

NATURAL REMEDY

STIMULATES HEALING

Recommended by Plastic Surgeons

Homeopathic Medicine

120 Sublingual Tablets

Arnica Montana 30X HPUS

ARNICA MONTANA
arnica montana tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:65111-005
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	30 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MANNITOL (UNII: 3OWL53L36A)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSPOVIDONE (UNII: 2S7830E561)
COPOVIDONE (UNII: D9C330MD8B)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (TABLET)	Size	6mm
Flavor		Imprint Code	V
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:65111-005-66	120 in 1 BOTTLE; Type 0: Not a Combination Product	02/13/2014	05/27/2026

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		02/13/2014	05/27/2026

Labeler - Vitamedica Corporation (808198779)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(65111-005) , api manufacture(65111-005) , label(65111-005) , pack(65111-005)

Drug Facts