Tinnitus Relief
- Product NDC
- 57955-0275
- 11-digit product format
- 579550275
- Labeler code
- 57955
- Product ID
- 57955-0275_6e7194e0-cc4c-45b5-b131-32aca334fc1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- arnica montana, calcarea carbonica, chenopodium anthelminticum, chininum salicylicum, cimicifuga racemosa, coffea tosta, kali iodatum, kalmia latifolia, magnesia carbonica, manganum aceticum, manganum carbonicum, mercurius vivus, natrum salicylicum, salicylicum acidum, thiosinaminum, thyroidinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-11-06
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; DYSPHANIA AMBROSIOIDES; QUININE SALICYLATE; BLACK COHOSH; COFFEA ARABICA SEED, ROASTED; POTASSIUM IODIDE; KALMIA LATIFOLIA LEAF; MAGNESIUM CARBONATE; MANGANESE ACETATE TETRAHYDRATE; MANGANESE CARBONATE; MERCURY; SODIUM SALICYLATE; SALICYLIC ACID; ALLYLTHIOUREA; THYROID, UNSPECIFIED
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| dea2eded-d1e7-46bb-9a3d-f8dc20de6277 | Product name | 1 | 20190408 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57955-0275-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b2cf-f424-e053-dadaa90a57ce | Tinnitus Relief™ |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57955-0275-2 | Tinnitus Relief | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 57955-0275 | TINNITUS RELIEF (ARNICA MONTANA, CALCAREA CARBONICA, CHENOPODIUM ANTHELMINTICUM, CHININUM SALICYLICUM, CIMICIFUGA RACEMOSA, COFFEA TOSTA, KALI IODATUM, KALMIA LATIFOLIA, MAGNESIA CARBONICA, MANGANUM ACETICUM, MANGANUM CARBONICUM, MERCURIUS VIVUS, NATRUM SALICYLICUM, SALICYLICUM ACIDUM, THIOSINAMINUM, THYROIDINUM) LIQUID [KING BIO INC.] | 1 | Legacy NDC, 1 package rows | 20150304_1605d4b0-4be3-4da8-9792-fa0708e24422.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 57955-0275-2 | 57955027502 | 59 mL in 1 BOTTLE, SPRAY | 59 ml | Historical |