ring relief

Generic: arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea -

Labeler: trp company
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name ring relief
Generic Name arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea -
Labeler trp company
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

allylthiourea 6 [hp_X]/1, arnica montana 6 [hp_X]/1, calcium sulfide 13 [hp_X]/1, hypericum perforatum 6 [hp_X]/1, lycopodium clavatum spore 12 [hp_X]/1, mercurius solubilis 13 [hp_X]/1, salicylic acid 6 [hp_X]/1, silicon dioxide 13 [hp_X]/1

Manufacturer
TRP Company

Identifiers & Regulatory

Product NDC 17312-023
Product ID 17312-023_4606551b-3bef-8c1b-e063-6394a90a0160
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2011-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 17312023
Hyphenated Format 17312-023

Supplemental Identifiers

UPC
0858961001150
UNII
706IDJ14B7 O80TY208ZW 1MBW07J51Q XK4IUX8MNB C88X29Y479 324Y4038G2 O414PZ4LPZ ETJ7Z6XBU4

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ring relief (source: ndc)
Generic Name arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_X]/1
  • 13 [hp_X]/1
  • 12 [hp_X]/1
source: ndc
Packaging
  • 1 BOTTLE in 1 PACKAGE (17312-023-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (8)

allylthiourea (6 [hp_X]/1) arnica montana (6 [hp_X]/1) calcium sulfide (13 [hp_X]/1) hypericum perforatum (6 [hp_X]/1) lycopodium clavatum spore (12 [hp_X]/1) mercurius solubilis (13 [hp_X]/1) salicylic acid (6 [hp_X]/1) silicon dioxide (13 [hp_X]/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4606551b-3bef-8c1b-e063-6394a90a0160", "openfda": {"upc": ["0858961001150"], "unii": ["706IDJ14B7", "O80TY208ZW", "1MBW07J51Q", "XK4IUX8MNB", "C88X29Y479", "324Y4038G2", "O414PZ4LPZ", "ETJ7Z6XBU4"], "spl_set_id": ["aa2cd967-3c27-4afe-8751-7ea50ab62913"], "manufacturer_name": ["TRP Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 PACKAGE (17312-023-14)  / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE", "package_ndc": "17312-023-14", "marketing_start_date": "20111201"}], "brand_name": "Ring Relief", "product_id": "17312-023_4606551b-3bef-8c1b-e063-6394a90a0160", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "17312-023", "generic_name": "ARNICA MONTANA - CALCIUM SULFIDE - HYPERICUM PERFORATUM - LYCOPODIUM CLAVATUM SPORE - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA -", "labeler_name": "TRP Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ring Relief", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "6 [hp_X]/1"}, {"name": "ARNICA MONTANA", "strength": "6 [hp_X]/1"}, {"name": "CALCIUM SULFIDE", "strength": "13 [hp_X]/1"}, {"name": "HYPERICUM PERFORATUM", "strength": "6 [hp_X]/1"}, {"name": "LYCOPODIUM CLAVATUM SPORE", "strength": "12 [hp_X]/1"}, {"name": "MERCURIUS SOLUBILIS", "strength": "13 [hp_X]/1"}, {"name": "SALICYLIC ACID", "strength": "6 [hp_X]/1"}, {"name": "SILICON DIOXIDE", "strength": "13 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20111201", "listing_expiration_date": "20261231"}