SORE MUSCLE AND JOINT PAIN RELIEF- arnica montana and hypericum perforatum cream

SORE MUSCLE AND JOINT PAIN RELIEF by

Drug Labeling and Warnings

SORE MUSCLE AND JOINT PAIN RELIEF by is a Homeopathic medication manufactured, distributed, or labeled by PUREMEDY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS

ARNICA MONTANA HPUS (1X)

HYPERICUM PERFORATUM (ST. JOHN'S WORT) HPUS (1X)

PURPOSE

PURPOSE

MUSCLE SORENESS

JOINT AND NERVE PAIN RELIEF

INDICATIONS & USAGE

USES: FOR RELIEF OF MUSCLE, JOINT ACHES AND STIFFNESS

DOSAGE & ADMINISTRATION

DIRECTIONS: APPLY TOPICALLY AS NEEDED.

INACTIVE INGREDIENT

OTHER INGREDIENTS: SPRING WATER, OLIVE OIL, BALSAM FIR, CANDELILA WAX, ELDER, CALENDULA, TUMERIC POWDER, CAYENNE PEPPER, FIR NEEDLE OIL, EUCALYPTUS OIL

WARNINGS

WARNING: DO NOT USE IF ALLERGIC TO OR SENSITIVE TO ANY INGREDIENT IN THIS CREAM. IF CONDITION PERSISTS OR WORSENS SEE A DOCTOR. AVOID CONTACT WITH EYES AND OPEN WOUNDS. USE ONLY AS DIRECTED.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SORE MUSCLE AND JOINT PAIN RELIEF 
arnica montana and hypericum perforatum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52810-703
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	1 [hp_X]  in 100 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	1 [hp_X]  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
OLIVE OIL (UNII: 6UYK2W1W1E)
ABIES BALSAMEA LEAF OIL (UNII: 2FGT9T2SQC)
CANDELILLA WAX (UNII: WL0328HX19)
SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
TURMERIC (UNII: 856YO1Z64F)
CAPSICUM (UNII: 00UK7646FG)
EUCALYPTUS OIL (UNII: 2R04ONI662)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52810-703-11	30 mL in 1 JAR; Type 0: Not a Combination Product	10/17/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/17/2013

Labeler - PUREMEDY (003552251)

Establishment
Name	Address	ID/FEI	Business Operations
PUREMEDY		003552251	manufacture(52810-703)