TOXO HOMO
- Product NDC
- 43742-2002
- 11-digit product format
- 437422002
- Labeler code
- 43742
- Product ID
- 43742-2002_639b723a-bdad-4e0e-9c2e-f1182f4e927c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOXOPLASMA GONDII DNA
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-12-21
- Substance
- TOXOPLASMA GONDII DNA
- Active strength
- 15 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TOXO HOMO
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOXOPLASMA GONDII DNA | 15 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JMX3ACIU25 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43742-2002-1 | TOXO HOMO | 30 mL in 1 BOTTLE, PLASTIC | LIQUID | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43742-2002 | TOXO HOMO (TOXOPLASMA GONDII DNA) LIQUID [DESERET BIOLOGICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240501_149b421a-51f0-409b-8913-c367256488fa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-2002-1 | 43742200201 | 30 mL in 1 BOTTLE, PLASTIC (43742-2002-1) | 30 ml | 2020-12-21 | 0000-00-00 | No | No | Current |