NYLOXIN
- Product NDC
- 47219-253
- 11-digit product format
- 472190253
- Labeler code
- 47219
- Product ID
- 47219-253_8d5c7de0-ddbd-11de-9b36-0002a5d5c51b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAJA NAJA VENOM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- RECEPTOPHARM INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-08-25
- Marketing end
- 0000-00-00
- Substance
- NAJA NAJA VENOM
- Active strength
- 60 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 |
|---|
| 47219-253-20 | NYLOXINStage 3 Pain Relief | 60 mL in 1 BOTTLE, DISPENSING | GEL | 60 | | 1 |
| 47219-253-20 | NYLOXINStage 3 Pain Relief | 1 in 1 BOX | GEL | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47219-253 | NYLOXIN STAGE 3 PAIN RELIEF (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC] | 1 | Legacy NDC, 2 package rows | 20110113_883f49a0-ddbd-11de-be01-0002a5d5c51b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 47219-253-20 | 47219025320 | 60 mL in 1 BOTTLE, DISPENSING | 60 ml | Historical |