Allergy Care
NDC 70163-0035, Adrenalinum, Ragweed, Pollen (Ambrosia Artemisiaefolia), Apis Mellifica, Echinacea (Angustifolia), Histaminum Hydrochloricum, Ledum Palustre, Lycopodium Clavatum, Natrum Muriaticum, Sulphur, liquid, from NaturalCare.
- Product NDC
- 70163-0035
- Status
- Listed
- Labeler
- NaturalCare
- Dosage form
- LIQUID
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70163-0035 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- EPINEPHRINE6 [hp_X]/mL
- AMBROSIA ARTEMISIIFOLIA POLLEN6 [hp_X]/mL
- APIS MELLIFERA6 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE4 [hp_X]/mL
- HISTAMINE DIHYDROCHLORIDE12 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG8 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE6 [hp_X]/mL
- SODIUM CHLORIDE8 [hp_X]/mL
- SULFUR6 [hp_X]/mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Pollen [CS]; Standardized Insect Venom Allergenic Extract [EPC]; Standardized Pollen Allergenic Extract [EPC]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70163-0035-2 | 70163003502 | 1 BOTTLE, DROPPER in 1 CARTON (70163-0035-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0035-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 70163-0035 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70163-0035 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70163-0035. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.