TINNITUS CONTROL
- Product NDC
- 43695-0009
- 11-digit product format
- 436950009
- Labeler code
- 43695
- Product ID
- 43695-0009_f0c7c0f2-0181-406c-a692-8a9d1c637879
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NOT APPLICABLE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Pacific Naturals
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-10-14
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA; QUININE SULFATE; IRON; POTASSIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; PULSATILLA VULGARIS; SILICON DIOXIDE; ALLYLTHIOUREA
- Active strength
- 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43695-0009-1 | TINNITUS CONTROL | 30 mL in 1 BOTTLE, SPRAY | LIQUID | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43695-0009 | TINNITUS CONTROL (NOT APPLICABLE) LIQUID [PACIFIC NATURALS] | 1 | Legacy NDC, 1 package rows | 20141022_d7a5c0ad-deb2-4a8e-afc8-6d630509e026.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 43695-0009-1 | 43695000901 | 30 mL in 1 BOTTLE, SPRAY | 30 ml | Historical |