GUNA-TF PAPILLOMA
- Product NDC
- 17089-281
- 11-digit product format
- 170890281
- Labeler code
- 17089
- Product ID
- 17089-281_69423426-fa1c-4b19-bbe5-fe63ddb688e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HUMAN PAPILLOMAVIRUS
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2008-04-16
- Marketing end
- 0000-00-00
- Substance
- HUMAN PAPILLOMAVIRUS
- Active strength
- 7 [hp_X]/4600mg
- 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 |
|---|
| 17089-281-10 | GUNA-TF PAPILLOMA | 4600 mg in 1 BOTTLE | CAPSULE, GELATIN COATED | 4600 | | 1 |
| 17089-281-10 | GUNA-TF PAPILLOMA | 1 in 1 BOX | CAPSULE, GELATIN COATED | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17089-281 | GUNA-TF PAPILLOMA (HUMAN PAPILLOMAVIRUS) CAPSULE, GELATIN COATED [GUNA SPA] | 1 | Legacy NDC, 2 package rows | 20100331_9badc0cf-f62c-4444-a66d-1204c3397bb7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17089-281-10 | 17089028110 | 4600 mg in 1 BOTTLE | 4600 mg | Historical |