Indications and uses
Temporarily reduces joint inflammation and pain and general associated pain.
Temporarily reduces joint inflammation and pain and general associated pain.
Dissolve one (1) strip under tongue daily. It may take up to 15 doses to start relief.
For oral use only
If symptoms persist stop using this product and consult a physician
Side effects may include headache, nausea, sore throat
Keep out of reach of children
Naja Naja H 10X
Carboxymethyelcellulose, sodium chloride 0.9%, water, natural orange flavorings, sucrose , thimerosol
Immune Modulator
Not for use by pregnant or nursing women
Temporarily reduces joint inflammation and pain and general associated pain.
Dissolve one (1) strip under tongue daily. It may take up to 15 doses to start relief.
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72295-002-03 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-3274-f274-e053-dbdaa90a6471 | V 7 SERPENTES Immune Modulatory Treatment |
| 72295-002-03 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-3274-f274-e053-dbdaa90a6471 | V 7 SERPENTES Immune Modulatory Treatment |
| 72295-002-03 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-3274-f274-e053-dbdaa90a6471 | V 7 SERPENTES Immune Modulatory Treatment |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72295-002-03 | V 7 SERPENTES | 15 [hp_X] in 1 POUCH | STRIP | 15 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72295-002 | 72295-002-03 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| WATER | 059QF0KO0R | IACT |
| THIMEROSAL | 2225PI3MOV | IACT |
| NAJA NAJA VENOM | ZZ4AG7L7VM | ACTIB |
| CARBOXYMETHYLCELLULOSE | 05JZI7B19X | IACT |
| SUCROSE | C151H8M554 | IACT |
| ORANGE OIL | AKN3KSD11B | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 6a9dbf2c-6210-5b35-e053-2a91aa0a9245 | 6a9dbf2c-620f-5b35-e053-2a91aa0a9245 | 2018-05-02 | Warnings | 6a9dbf2c-6210-5b35-e053-2a91aa0a9245 6a9dbf2c-620f-5b35-e053-2a91aa0a9245 |
Adverse event summaries are temporarily unavailable. Other product information remains available.