17089-476 : Guna Hay Fever Relief Oral Pellet
| NDC: | 17089-476 |
| Labeler: | Guna Spa |
| Product Type: | Human OTC Drug |
| Drug Name: | Guna Hay Fever Relief |
| Dosage Form: | Oral Pellet |
| Rev. Date: |
NDC Package Codes:
- 17089-476-20: 2 TUBE IN 1 BOX (17089‑476‑20) > 4 G IN 1 TUBE
- 17089-476-21: 1 TUBE IN 1 BOX (17089‑476‑21) > 4 G IN 1 TUBE
Active Ingredients:
- Strychnos Nux-vomica Seed
- Histamine Dihydrochloride
- Manganese
- Schoenocaulon Officinale Seed
- Onion
- Apis Mellifera
- Silver Nitrate
- Euphrasia Stricta
- Galphimia Glauca Flowering Top
- Sulfur
- Arsenic Trioxide
Dosage Strength:
- 4 [hp_X]/4g
- 200 [hp_X]/4g
- 8 [hp_X]/4g
- 6 [hp_X]/4g
- 30 [hp_X]/4g
- 200 [hp_X]/4g
- 6 [hp_X]/4g
- 5 [hp_X]/4g
- 4 [hp_X]/4g
- 30 [hp_X]/4g
- 30 [hp_X]/4g
Pharmaceutical Classes:
- Allergens [CS]
- Allergens [CS]
- Bee Venoms [CS]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Food Allergenic Extract [EPC]
- Non-Standardized Plant Allergenic Extract [EPC]
- Plant Proteins [CS]
- Seed Storage Proteins [CS]
- Standardized Insect Venom Allergenic Extract [EPC]
- Vegetable Proteins [CS]
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
