GUNA-IL 12
- Product NDC
- 17089-390
- 11-digit product format
- 170890390
- Labeler code
- 17089
- Product ID
- 17089-390_ed81a1dd-c092-49a5-e053-2995a90aad04
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- INTERLEUKIN-12 HUMAN RECOMBINANT
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2008-06-17
- Substance
- INTERLEUKIN-12 HUMAN RECOMBINANT
- Active strength
- 4 [hp_C]/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GUNA-IL 12
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| INTERLEUKIN-12 HUMAN RECOMBINANT | 4 [hp_C]/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 02FXP10O2U |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17089-390-18 | GUNA-IL 12 | 30 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 30 | | 5 |
| 17089-390-18 | GUNA-IL 12 | 1 in 1 BOX | SOLUTION/ DROPS | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17089-390 | GUNA-IL 12 (INTERLEUKIN-12 HUMAN RECOMBINANT) SOLUTION/ DROPS [GUNA SPA] | 5 | Current NDC, Legacy NDC, 2 package rows | 20221116_6a2513f0-cda9-4121-9581-5fd9078bd299.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17089-390-18 | 17089039018 | 1 BOTTLE, DROPPER in 1 BOX (17089-390-18) / 30 mL in 1 BOTTLE, DROPPER | 2010-06-10 | 0000-00-00 | No | No | Current |