Label: T-RELIEF PET PAIN- arnica montana, calendula officinalis flowering top, hamamelis virginiana root bark stem bark, baptisia tinctoria root, bellis perennis, echinacea angustifolia, aconitum napellus, matricaria chamomilla, achillea millefolium, atropa belladonna, hypericum perforatum and comfrey root solution/ drops
- NDC Code(s): 62795-3005-4
- Packager: MediNatura New Mexico Inc
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated September 18, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Warnings
- Indication:
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Directions
Directions: Administer directly into the mouth with a little water preferably
between meals. If this is difficult, drops can be mixed with a small amount
of water or food.–
Dose: 3 times per day – Cats & dogs: Newborn – 5 drops. Weaned – 10
drops. Adult cat – 10 drops. Adult dog (small) – 10 drops. Adult dog (large)
– ½ dropperful. Horses: Foals – Two, ½ dropperfuls. Adult horse – Three,
½ dropperfuls. Other animal: Consult your veterinarian.– - Inactives
- Keep out of reach of children.
- Purpose
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Active Ingredients
Each 50mL contains: *Aconitum napellus 3X 10%,
*Arnica montana 3X 50%, *Arnica montana 6X 7%, *Arnica montana
10X 2%, *Baptisia tinctoria 2X 2%, *Belladonna 3X 2.6%, *Bellis
perennis 2X 2%, *Calendula officinalis 2X 3.4%, *Chamomilla 2X 1%,
*Echinacea 2X 2%, *Hamamelis virginiana 2X 3.3%, *Hypericum
perforatum 3X 2.7%, *Millefolium 2X - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
T-RELIEF PET PAIN
arnica montana, calendula officinalis flowering top, hamamelis virginiana root bark stem bark, baptisia tinctoria root, bellis perennis, echinacea angustifolia, aconitum napellus, matricaria chamomilla, achillea millefolium, atropa belladonna, hypericum perforatum and comfrey root solution/ dropsProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:62795-3005 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 3 [hp_X] in 50 mL CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X] in 50 mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X] in 50 mL BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 2 [hp_X] in 50 mL BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) BELLIS PERENNIS 2 [hp_X] in 50 mL ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 2 [hp_X] in 50 mL ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 3 [hp_X] in 50 mL MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ) MATRICARIA CHAMOMILLA 2 [hp_X] in 50 mL ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK) ACHILLEA MILLEFOLIUM 2 [hp_X] in 50 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 3 [hp_X] in 50 mL HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 3 [hp_X] in 50 mL RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 4 [hp_X] in 50 mL COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 8 [hp_X] in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID ACETATE (UNII: DSO12WL7AU) Sodium Benzoate (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-3005-4 1 in 1 CARTON 1 50 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/05/2022 Labeler - MediNatura New Mexico Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura New Mexico Inc 102783016 api manufacture, manufacture