Label: THYROID SOOTHE- chamomilla, iodium, lycopus, nux vom, zingiber granule
- NDC Code(s): 68703-025-20
- Packager: Native Remedies, LLC
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated July 11, 2012
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- PURPOSE
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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INFORMATION FOR OWNERS/CAREGIVERS
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
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Native Remedies, LLC
6531 Park of Commerce Blvd.
Suite 160
Boca Raton, FL 33487
Phone: +1.877.289.1235
International: +1.561.999.8857
- STORAGE AND HANDLING
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THYROID SOOTHE
chamomilla, iodium, lycopus, nux vom, zingiber granuleProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:68703-025 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA 30 [hp_C] in 40 mg IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 30 [hp_C] in 40 mg LYCOPUS VIRGINICUS (UNII: TWH5125Q6F) (LYCOPUS VIRGINICUS - UNII:TWH5125Q6F) LYCOPUS VIRGINICUS 6 [hp_C] in 40 mg STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 30 [hp_C] in 40 mg Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) STARCH, CORN (UNII: O8232NY3SJ) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SUCROSE (UNII: C151H8M554) Product Characteristics Color white (White granules) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68703-025-20 20000 mg in 1 BOTTLE, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/01/2012 Labeler - Native Remedies, LLC (192014186) Registrant - Native Remedies, LLC (192014186) Establishment Name Address ID/FEI Business Operations King Bio 617901350 api manufacture, manufacture