ARNICA MONTANA 30 [hp_C]

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Drug Information

Imprint:	B;T
Shape:	C48348
Color:	C48325
Ingredients:
Size:	6.00
Score:	1
Rxtty:
Author:	Nature's Way Products, Inc.
Inactive Ingredients:	CELLULOSE, MICROCRYSTALLINE / LACTOSE / MAGNESIUM STEARATE / CROSCARMELLOSE SODIUM>

Active Ingredient

Arnica Montana 30C

Inactive Ingredients
CELLULOSE

LACTOSE MONOHYDRATE

MAGNESIUM STEARATE

SODIUM CROSCARMELLOSEÂ
Dosage and Administration

Adults or children over 2 years:Â Take 3 tablets 1 to 3 times per day.

Allow to dissolve under tongue.Â

Indications and Usage
Temporarily relieves minor muscle or joint aches and pains from strains, sprains, bruises, backache, over extertion.

Purpose
For the temporary relief of minor muscle or joint aches and pains from strains, sprains, bruises, backache and over exertion.
Warnings

Do not use this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor.Â
When usingÂ

When using this product, if pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a serous condition.
Pregnancy or Breast Feeding

If you are pregnant or breast-feeding, ask a healthcare professional before use.
Keep out of reach of children

Keep out of reach of children
Overdose

In case of overdose, seek medical help or contact a Posion Control Center immediately.
PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARNICA MONTANAÂ
arnica montana tablet

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

Ingredient Name	Strength
Inactive Ingredients
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)	Â
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)	Â
MAGNESIUM STEARATE (UNII: 70097M6I30)	Â
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)	Â

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:53499-3571-2	100 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/2006	03/31/2027
2	NDC:53499-3571-3	250 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/2006	03/31/2027

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		01/01/2006	03/31/2027

Labeler -Â Schwabe North America, Inc. (831153908)

Name	Address	ID/FEI	Business Operations
Establishment
Schwabe Mexico, S.A. deC.V.		812805901	manufacture(53499-3571)