Hot Spot Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Hot Spot Relief

Native Remedies, LLC

Hot Spot Relief




FULL PRESCRIBING INFORMATION

Purpose

Relieves symptoms associated with hot spots

Active ingredient

Drug Facts
Active Ingredients:
Equal volumes of each ingredients in 12X, 30X and LM1 potencies: Alumina, Antimonium tartaricum, Dolichos pruriens, Fagopyrum esculentum, Graphites, Muriaticum acidum, Oleander, Rhus toxicodendron, Urtica urens

Uses

Uses: For temporary relief of symptoms associated with hot spots, including itching, soreness and redness

Warnings: If symptoms persist or worsen, seek advice of a veterinarian

If pet is pregnant or nursing, give only on advice of a veterinarian

Keep this and all medication out of reach of children

Directions: Initially, depress pump until primed. Hold close and spray directly into pet's mouth, or spray onto its food or water. Use 3 times daily. Cats and dogs under 20 lbs: 2 sprays. Dogs 20-50 lbs: 3 sprays. Dogs over 50 lbs: 4 sprays

Inactive Ingredients: Citric acid, potassium sorbate, purified water

The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.petalive.com

Distributed by
Native Remedies, LLC
6531 Park of Commerce Blvd
Suite 160
Boca Raton, FL 33487
Phone: 1.800.683.1235
International: +1.561.999.8857

Contains no flavors or artificial colors. No gluten added

Tamper resistant for your protection. Use only if safety seal is intact

Hot Spot Relief

Hot Spot Relief

Alumina, Antimonium tartaricum, Dolichos pruriens, Fagopyrum esculentum, Graphites, Muriaticum acidum, Oleander, Rhus toxicodendron, Urtica urens SPRAY

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:68703-145
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALUMINUM OXIDE 12 [hp_X]
Antimony Potassium Tartrate ANTIMONY CATION (3+) 12 [hp_X]
MUCUNA PRURIENS FRUIT TRICHOME MUCUNA PRURIENS FRUIT TRICHOME 12 [hp_X]
FAGOPYRUM ESCULENTUM FAGOPYRUM ESCULENTUM 12 [hp_X]
Graphite GRAPHITE 12 [hp_X]
HYDROCHLORIC ACID 12 [hp_X]
Nerium Oleander Leaf NERIUM OLEANDER LEAF 12 [hp_X]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 12 [hp_X]
Urtica Urens URTICA URENS 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68703-145-59 59 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-11-18


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