HAY FEVER 1
- Product NDC
- 64117-203
- 11-digit product format
- 641170203
- Labeler code
- 64117
- Product ID
- 64117-203_97040e0b-263e-4352-bb42-8f883120b419
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AMBROSIA ARTEMISIIFOLIA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Natural Health Supply
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1998-06-04
- Marketing end
- 0000-00-00
- Substance
- AMBROSIA ARTEMISIIFOLIA
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 64117-203-01 | HAY FEVER 1 | 1.875 mL in 1 BOTTLE, GLASS | PELLET | 1.875 | | 2 |
| 64117-203-02 | HAY FEVER 1 | 7.5 mL in 1 BOTTLE, GLASS | PELLET | 7.5 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64117-203 | HAY FEVER 1 (AMBROSIA ARTEMISIIFOLIA) PELLET [NATURAL HEALTH SUPPLY] | 2 | Legacy NDC, 2 package rows | 20190225_31bcb1e8-758c-4722-a4fb-cc5fba27e2c9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64117-203-01 | 64117020301 | 1.875 mL in 1 BOTTLE, GLASS (64117-203-01) | 1.875 ml | 1998-06-04 | 0000-00-00 | No | No | Current |
| 64117-203-02 | 64117020302 | 7.5 mL in 1 BOTTLE, GLASS (64117-203-02) | 7.5 ml | 1998-06-04 | 0000-00-00 | No | No | Current |