DOCTOR HOYS ARNICA BOOST RECOVERY- arnica montana gel

Doctor Hoys Arnica Boost Recovery by

Drug Labeling and Warnings

Doctor Hoys Arnica Boost Recovery by is a Homeopathic medication manufactured, distributed, or labeled by Dynamic Blending Specialists, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active ingredients:

Arnica Montana 1X HPUS (5%)

Purpose:

Anit-inflammatory

Uses:

Temporary relief of minor aches and pains associated with: scrapes  bruising  joints  sprains  inflammation

Warnings:

For external use only

Use as directed 

Avoid contact with eyes

Keep Out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately 

If pregnant or breast feeding,

ask a health professional before use

Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days.

Directions:

For adults and children 2 years and older: Apply generously to affected and surrounding areas 

Repeat use as needed 

For children under 2 years of age: Consult a physician before use.

Inactive ingedients:

Aloe Barbadensis Leaf Juice, Anthemis Nobilis (Chamomile) Flower Oil, Argania Spinosa Kernel (Argan) Oil, Calendula Officinalis, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Olivate, Cetyl Alcohol, DL Panthenol, Glycerin, Glyceryl Stearate, Hamamelis Virginiana (Witch Hazel), Hypericum Perforatum (St. Johns Wort), MSM (Methyl Sulfonyl Methane), Phenoxyethanol(and) Ethylhexylglycerin, Simmondsia Chinensis (Jojoba) Seed Oil, Squalane, Stearic Acid, Triethanolamine, Tocopherol, Water.

75638-009-00

75638-009-01

75638-009-02

INGREDIENTS AND APPEARANCE

DOCTOR HOYS ARNICA BOOST RECOVERY 
arnica montana gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75638-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
ARGAN OIL (UNII: 4V59G5UW9X)
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SAFFLOWER OIL (UNII: 65UEH262IS)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CETYL ALCOHOL (UNII: 936JST6JCN)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
JOJOBA OIL (UNII: 724GKU717M)
SQUALANE (UNII: GW89575KF9)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75638-009-00	89 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023
2	NDC: 75638-009-01	177 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023
3	NDC: 75638-009-02	946 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/01/2023

Labeler - Dynamic Blending Specialists, Inc. (085704438)