NYLOXIN
- Product NDC
- 47219-251
- 11-digit product format
- 472190251
- Labeler code
- 47219
- Product ID
- 47219-251_7256a740-d931-11de-ae13-0002a5d5c51b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAJA NAJA VENOM
- Dosage form
- SPRAY, METERED
- Route
- ORAL
- Labeler
- RECEPTOPHARM INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-08-25
- Marketing end
- 0000-00-00
- Substance
- NAJA NAJA VENOM
- Active strength
- 280 ug/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47219-251-10 | NYLOXINStage 3 Pain Relief | 1 in 1 BOX | SPRAY, METERED | 1 | | 1 |
| 47219-251-10 | NYLOXINStage 3 Pain Relief | 30 mL in 1 BOTTLE, SPRAY | SPRAY, METERED | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47219-251 | NYLOXIN STAGE 3 PAIN RELIEF (NAJA NAJA VENOM) SPRAY, METERED [RECEPTOPHARM INC] | 1 | Legacy NDC, 2 package rows | 20110113_6d4ecfc0-d931-11de-beed-0002a5d5c51b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 47219-251-10 | 47219025110 | 1 in 1 BOX | Historical |