Allergy Nosode
- Product NDC
- 63083-4017
- 11-digit product format
- 630834017
- Labeler code
- 63083
- Product ID
- 63083-4017_8f6adf24-31cc-4860-b955-0076730f68ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allergy Nosode
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- CALCIUM SULFIDE; FRAXINUS LATIFOLIA WHOLE; GUAIAC; HISTAMINE; HOUSE DUST; LUFFA OPERCULATA FRUIT; MEDICAGO SATIVA WHOLE; POTASSIUM DICHROMATE; SILICON DIOXIDE; STACHYBOTRYS CHARTARUM; TARAXACUM OFFICINALE
- Active strength
- 12; 12; 6; 12; 12; 6; 12; 30; 12; 12; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], House Dust [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized House Dust Allergenic Extract [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allergy Nosode
- Brand name suffix
- 4017
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM SULFIDE | 12 [hp_X]/59mL |
| FRAXINUS LATIFOLIA WHOLE | 12 [hp_X]/59mL |
| GUAIAC | 6 [hp_X]/59mL |
| HISTAMINE | 12 [hp_X]/59mL |
| HOUSE DUST | 12 [hp_X]/59mL |
| LUFFA OPERCULATA FRUIT | 6 [hp_X]/59mL |
| MEDICAGO SATIVA WHOLE | 12 [hp_X]/59mL |
| POTASSIUM DICHROMATE | 30 [hp_X]/59mL |
| SILICON DIOXIDE | 12 [hp_X]/59mL |
| STACHYBOTRYS CHARTARUM | 12 [hp_X]/59mL |
| TARAXACUM OFFICINALE | 12 [hp_X]/59mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1MBW07J51Q, 024W88F557, 03C8A0DFJ8, 820484N8I3, EYO007VX98, C4MO6809HU, DJO934BRBD, T4423S18FM, ETJ7Z6XBU4, HJ4L70T1ZP, 39981FM375 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63083-4017-2 | Allergy Nosode4017 | 59 mL in 1 BOTTLE, DROPPER | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-4017 | ALLERGY NOSODE 4017 (ALLERGY NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220301_da9145a5-42e9-4dba-9d11-195848e628a4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-4017-2 | 63083401702 | 59 mL in 1 BOTTLE, DROPPER (63083-4017-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |