Topricin
Aesculus Hippocastanum, Arnica Montana, Belladonna, Calendula Officinalis, Crotalus Horridus, Echinacea, Graphites, Heloderma Horridum, Lachesis Mutus, Naja Tripudians, Phosphorus, Rhus Toxicodendron, Ruta Graveolens, Sulfur
Topical Biomedics, Inc.
Human Otc Drug
NDC 61500-5547Topricin also known as Aesculus Hippocastanum, Arnica Montana, Belladonna, Calendula Officinalis, Crotalus Horridus, Echinacea, Graphites, Heloderma Horridum, Lachesis Mutus, Naja Tripudians, Phosphorus, Rhus Toxicodendron, Ruta Graveolens, Sulfur is a human otc drug labeled by 'Topical Biomedics, Inc.'. National Drug Code (NDC) number for Topricin is 61500-5547. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Topricin drug includes Aesculus Hippocastanum Flower - 6 [hp_X]/227g Arnica Montana - 6 [hp_X]/227g Atropa Belladonna - 6 [hp_X]/227g Calendula Officinalis Flowering Top - 4 [hp_X]/227g Crotalus Horridus Horridus Venom - 8 [hp_X]/227g Echinacea Angustifolia - 4 [hp_X]/227g Graphite - 6 [hp_X]/227g Heloderma Horridum Venom - 8 [hp_X]/227g Lachesis Muta Venom - 8 [hp_X]/227g Naja Naja Venom - 8 [hp_X]/227g and more. The currest status of Topricin drug is Active.
Drug Information:
| Drug NDC: | 61500-5547 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Topricin |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Aesculus Hippocastanum, Arnica Montana, Belladonna, Calendula Officinalis, Crotalus Horridus, Echinacea, Graphites, Heloderma Horridum, Lachesis Mutus, Naja Tripudians, Phosphorus, Rhus Toxicodendron, Ruta Graveolens, Sulfur |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Topical Biomedics, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cream |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | AESCULUS HIPPOCASTANUM FLOWER - 6 [hp_X]/227g
ARNICA MONTANA - 6 [hp_X]/227g
ATROPA BELLADONNA - 6 [hp_X]/227g
CALENDULA OFFICINALIS FLOWERING TOP - 4 [hp_X]/227g
CROTALUS HORRIDUS HORRIDUS VENOM - 8 [hp_X]/227g
ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/227g
GRAPHITE - 6 [hp_X]/227g
HELODERMA HORRIDUM VENOM - 8 [hp_X]/227g
LACHESIS MUTA VENOM - 8 [hp_X]/227g
NAJA NAJA VENOM - 8 [hp_X]/227g
Load more...PHOSPHORUS - 9 [hp_X]/227g
RUTA GRAVEOLENS FLOWERING TOP - 6 [hp_X]/227g
SULFUR - 8 [hp_X]/227g
TOXICODENDRON PUBESCENS LEAF - 8 [hp_X]/227g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 18 May, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 01 Apr, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Listing Expiration Date: | 10 Jun, 2026 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Topical BioMedics, Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0609863010081
|
| UPC stands for Universal Product Code. |
| UNII: | KK0Z92II8M
O80TY208ZW
WQZ3G9PF0H
18E7415PXQ
YHA2XLJ956
VB06AV5US8
4QQN74LH4O
O9M1UQ4YIO
VSW71SS07I
ZZ4AG7L7VM
Load more...27YLU75U4W
N94C2U587S
70FD1KFU70
6IO182RP7A
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 61500-5547-0 | 2 g in 1 PACKET (61500-5547-0) | 01 Jun, 2016 | 01 Apr, 2026 | No |
| 61500-5547-1 | 21 g in 1 TUBE (61500-5547-1) | 18 May, 2016 | 01 Apr, 2026 | No |
| 61500-5547-2 | 57 g in 1 TUBE (61500-5547-2) | 18 May, 2016 | 01 Apr, 2026 | No |
| 61500-5547-4 | 113 g in 1 JAR (61500-5547-4) | 18 May, 2016 | 01 Apr, 2026 | No |
| 61500-5547-8 | 454 g in 1 BOTTLE (61500-5547-8) | 18 May, 2016 | 01 Apr, 2026 | No |
| 61500-5547-9 | 227 g in 1 BOTTLE (61500-5547-9) | 18 May, 2016 | 01 Apr, 2026 | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose relieves pain of the achilles tendon, swelling of the feet after walking aids in treating injuries & bruising to muscles and joints aids in treating night leg cramps, restless leg and muscle spasms aids in rapid healing & treating dry skin on feet relief of impact injuries & sudden pain in feet & ankles relieves skin conditions relief of swelling & burning pain o the feet & toes relieves sudden sharp pain in the feet & ankle relieves nerve injury pain relief of coldness and cramping of the feet relief of pain for sprains and joint pain of the feet, heel and post-surgical pain relief of pain, soreness and bruising of the feet, ankle and shin relieves itching, cracking of the skin and joint pain in toes and feet
Product Elements:
Topricin aesculus hippocastanum, arnica montana, belladonna, calendula officinalis, crotalus horridus, echinacea, graphites, heloderma horridum, lachesis mutus, naja tripudians, phosphorus, rhus toxicodendron, ruta graveolens, sulfur caprylhydroxamic acid lecithin, soybean medium-chain triglycerides glycerin peg-100 stearate water steareth-21 glyceryl monostearate hydrogenated palm kernel oil cetyl alcohol carbomer interpolymer type a (allyl sucrose crosslinked) sodium hydroxide glyceryl caprylate isopropyl myristate phosphorus phosphorus arnica montana arnica montana crotalus horridus horridus venom crotalus horridus horridus venom echinacea angustifolia echinacea angustifolia graphite graphite heloderma horridum venom heloderma horridum venom lachesis muta venom lachesis muta venom naja naja venom naja naja venom ruta graveolens flowering top ruta graveolens flowering top aesculus hippocastanum flower aesculus hippocastanum flower atropa belladonna atropa belladonna toxicodendron pubescens leaf toxicodendron pubescens leaf calendula officinalis flowering top calendula officinalis flowering top sulfur sulfur
Indications and Usage:
Uses rapid, moisturizing healing pain relief from trauma injuries of the foot, ankle and lower extremity. reduces swelling, numbness and burning pain associated with: joint pain in the toes, feet and ankles heel pain/soreness (heel spurs) bunions pain/soreness (big toe) nerve pain (burning pain in feet) gout (pain in big toe) relieves arch pain, soft tissue pain, and ball of the foot relieves nerve pain between toes sports injuries, shin splints, ankle sprain, achilles tendonitis, plantar fasciitis tired aching feet, tarsal tunnel syndrome purpose relieves pain of the achilles tendon, swelling of the feet after walking aids in treating injuries & bruising to muscles and joints aids in treating night leg cramps, restless leg and muscle spasms aids in rapid healing & treating dry skin on feet relief of impact injuries & sudden pain in feet & ankles relieves skin conditions relief of swelling & burning pain o the feet & toes relieves sudden sharp pain in the feet & ankle relieves nerve in
Read more...jury pain relief of coldness and cramping of the feet relief of pain for sprains and joint pain of the feet, heel and post-surgical pain relief of pain, soreness and bruising of the feet, ankle and shin relieves itching, cracking of the skin and joint pain in toes and feet
Warnings:
Warnings for external use only. do not apply in eyes. ask doctor or pharmacist before using if you are taking prescription medication. ask a doctor before using if you are pregnant or nursing. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away. use only as directed. see doctor if pain persists for more than 3 days or worsens, new symptoms occur, redness or swelling are present because these could be signs of a more serious condition. before considering any self help regimen always consult your doctor, especially if you are taking a prescription medication.
Dosage and Administration:
Directions generously apply 3-4 times daily or more often if needed, 3 inches on and around affected area. massage in until absorbed, re-apply before bedtime and in the morning. use before and after sports work outs and competitions. apply immediately for acute trauma injuries (sprain, strain, bruise, and impact injuries).
Package Label Principal Display Panel:
Principal display panel us patents # 5,795,573 and #7,871,647 ndc# 61500-5547 topricin® foot pain relief cream moisturizing relief for foot, arch, hell, ankle and nerve pain ideal for diabetics homepathic net wt. 8.0 oz. paraben free principal label display