Label: EQUINE RESPIRATORY RELIEF- aconitum nap, belladonna, hepar sulph., silicea, merc sol , sulphur granule
- NDC Code(s): 50048-072-00
- Packager: W LAST CC
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated November 22, 2011
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- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- GENERAL PRECAUTIONS
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- WARNINGS
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INFORMATION FOR PATIENTS
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: 1.877.289.1235
International: + 1.561.999.8857
The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.
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INGREDIENTS AND APPEARANCE
EQUINE RESPIRATORY RELIEF
aconitum nap, belladonna, hepar sulph., silicea, merc sol , sulphur granuleProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50048-072 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 6 [hp_C] in 33.3 mg ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 30 [hp_C] in 33.3 mg CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFIDE 30 [hp_C] in 33.3 mg SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_X] in 33.3 mg MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 6 [hp_C] in 33.3 mg SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_C] in 33.3 mg Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50048-072-00 200000 mg in 1 BOTTLE, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2010 Labeler - W LAST CC (567284153) Registrant - W LAST CC (567284153) Establishment Name Address ID/FEI Business Operations W LAST CC 567284153 manufacture, api manufacture Establishment Name Address ID/FEI Business Operations FEELGOOD HEALTH 538418296 relabel