DOCTOR HOYS NATURAL ARNICA BOOST- hpus arnica montana cream

DOCTOR HOYS Natural Arnica Boost by

Drug Labeling and Warnings

DOCTOR HOYS Natural Arnica Boost by is a Homeopathic medication manufactured, distributed, or labeled by DOCTOR HOY'S, LLC, Specialty Formulations and Manufacturing LLC, Dynamic Blending Specialists, Inc., United Laboratories Manufacturing, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

Warnings: for external use only, avoid contact with eyes, Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately, if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician, Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use, do not bandage tightly

ACTIVE INGREDIENT

Active Ingredients Purpose

10% Arnica Montana 1X HPUS

INDICATIONS & USAGE

Directions: Use by itself or with DOCTOR HOY'S Natural Pain Relief Gel. For adults and children 2 years and older. "Children under 2 years of age: consult a doctor." For best results, apply generously to affected and surrounding areas. Repeat as needed.

Uses: for the temporary relief of minor aches and pains of muscles and joints due to: , inflammation, arthritis, sprains, strains, bruises

Inactive Ingredients: deionized water, hamamelis virginiana (witch hazel extract), isopropyl alcohol, cetyl alcohol, glycerin, tocopheryl acetate (vitamin E), aloe vera, argan oil, calendula oil, chamomile, hyperium Perforatum Extract, safflower oil, tilia cordata flower extract

PURPOSE

Uses: for the temporary relief of minor aches and pains of muscles and joints associated with: Inflammation, arthritis, sprains, strains, bruises, Expedites healing, Reduces swelling, Extends relief time, Absorbs quickly, Odorless

KEEP OUT OF REACH OF CHILDREN

Warnings: for external use only, avoid contact with eyes, Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately, if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician, Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use, do not bandage tightly

DOSAGE & ADMINISTRATION

Directions: Use by itself or with DOCTOR HOY'S Natural Pain Relief Gel. for adults and children 2 years and older. "Children under 2 years of age: consult a doctor." For best results, apply generously to affected and surrounding areas. Repeat as needed.

PRINCIPAL DISPLAY PANEL

An image/graphic of the product is included

INGREDIENTS AND APPEARANCE

DOCTOR HOYS NATURAL ARNICA BOOST 
hpus arnica montana cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10842-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW)	ARNICA MONTANA	5 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CHAMOMILE (UNII: FGL3685T2X)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
PANTHENOL (UNII: WV9CM0O67Z)
SAFFLOWER OIL (UNII: 65UEH262IS)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
WITCH HAZEL (UNII: 101I4J0U34)
CETYL ALCOHOL (UNII: 936JST6JCN)
JOJOBA OIL (UNII: 724GKU717M)
ARGAN OIL (UNII: 4V59G5UW9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10842-203-02	946 mL in 1 JUG; Type 0: Not a Combination Product	06/20/2019
2	NDC: 10842-203-01	89 mL in 1 TUBE; Type 0: Not a Combination Product	06/20/2019
3	NDC: 10842-203-03	1893 mL in 1 JUG; Type 0: Not a Combination Product	06/20/2019
4	NDC: 10842-203-04	6 mL in 1 PACKET; Type 0: Not a Combination Product	06/20/2019
5	NDC: 10842-203-06	177 mL in 1 TUBE; Type 0: Not a Combination Product	06/20/2019
6	NDC: 10842-203-08	89 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	06/20/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/20/2019

Labeler - DOCTOR HOY'S, LLC (791882322)