ACTIVMEND- arnica montana, hypericum perforatum, ledum palustre, rhus toxicodendron, ruta graveolens, natrum muraticum patch

ActivMend by

Drug Labeling and Warnings

ActivMend by is a Homeopathic medication manufactured, distributed, or labeled by Cearna, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Active Ingredients for Gels:

Arnica Montana 1M

Hypericum Perforatum 1M

Ledum Palustre 1M

Rhus toxicodendron 1M

Ruta graveolens 1M

Natrum Muraticum 2C

PURPOSE

Purpose:

Arnica Montana 1M...........................Bruising, muscle strain

Hypericum Perforatum 1M ...............Pain

Ledum Palustre 1M.........................Swelling, pain

Rhus toxicodendron 1M...................Sprains, strains, swelling, pain

Ruta graveolens 1M.........................Strains

Natrum Muraticum 2C .......................Sprains

Uses

For the reduction of swelling and pain associated with joint sprains, muscle strains, shin splints, dislocations, overuse injuries, and bruising.

Warnings

Warnings

For external use on intact skin only

• Use only as directed.
• Do not bandage tightly.
• Stop use and ask a doctor if condition worsens.
• Do not use in the eyes, over open wounds, or if you have unexpected bleeding.
• If pregnant or breast-feeding, ask a health professional before use.
• Do not use if you are allergic to any of this product's active or ingredients.

Do not use

Do not use:

Do not use in the eyes, over open wounds, or if you have unexpected bleeding

Do not use if pouch is opened or damaged.

Stop use and ask a doctor

​Stop use and ask a doctor if condition worsens

PREGNANCY OR BREAST FEEDING

I f pregnant or breast-feeding ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

Directions:

Adults and Children 12 years of age and over

• Clean and dry affected area.
• Remove patch from film.
• Place healing pads on intact skin.
• Wear one activMend patch up to 24 hours.

Children under 12 years of age - Consult a doctor

Other information

• Store at room temperature.
• Do not freeze.

Tightly reseal pouch containing unused patches.

Inactive ingredients

Glycerin
Dihydroxyaluminum aminoacetate (Al-glycinate)
Titanium dioxide (TiO2)
1,2-hexanediol
Sodium Carbomethylcellulose (CMC-Na)
Partially neutralized polyacrylate
Disodium Edetatate (EDTA-2Na)
Tartaric acid
Water
Ethanol

Questions?

Questions: 1-855-255-MEND (6363)

or email: Support@ActivMend.com

SPL UNCLASSIFIED SECTION

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Do not use if pouches are open.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACTIVMEND 
arnica montana, hypericum perforatum, ledum palustre, rhus toxicodendron, ruta graveolens, natrum muraticum patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76277-122
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	2 [hp_C]  in 1 g
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	1 [hp_M]  in 1 g
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	1 [hp_M]  in 1 g
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	1 [hp_M]  in 1 g
RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S)	RUTA GRAVEOLENS FLOWERING TOP	1 [hp_M]  in 1 g
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	1 [hp_M]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TARTARIC ACID (UNII: W4888I119H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76277-122-32	1 in 1 BOX	02/09/2021
1		5 in 1 POUCH
1		14 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/09/2021

Labeler - Cearna, Inc. (968104609)

Registrant - Cearna, Inc. (968104609)