Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Pollen Hayfever NDC 70163-0031
Epinephrine 6 [hp_X]/mL + 18 more ingredients · Liquid · Oral · NaturalCare
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70163-0031-2 | 7016300310270163003102 | 1 BOTTLE, DROPPER in 1 CARTON (70163-0031-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0031-1)Marketed from May 5, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Pollen Hayfever
- Generic name (nonproprietary)
- adrenalinum, allium cepa, ambrosia artemisiaefolia, arsenicum iodatum, mugwort pollen (artemisia vulgaris), bellis perennis, brassica spp, chenopodium album, euphrasia officinalis, histaminum hydrochloricum, alfalfa pollen (medicago sativa), phleum pratense, yellow dock pollen (rumex crispus), sabadilla, silicea, goldenrod pollen (solidago canadensis), dandelion pollen (taraxacum officinale), red clover pollen (trifolium pratense), xanthium strumarium
- Active ingredients
- Epinephrine — 6 [hp_X]/mLOnion — 6 [hp_X]/mLAmbrosia artemisiifolia whole — 12 [hp_X]/mLArsenic triiodide — 6 [hp_X]/mLArtemisia vulgaris pollen — 12 [hp_X]/mLBellis perennis whole — 12 [hp_X]/mLBrassica rapa subsp. Oleifera pollen — 12 [hp_X]/mLChenopodium album pollen — 12 [hp_X]/mLEuphrasia stricta — 6 [hp_X]/mLHistamine dihydrochloride — 12 [hp_X]/mLMedicago sativa pollen — 12 [hp_X]/mLPhleum pratense pollen — 12 [hp_X]/mLRumex crispus pollen — 12 [hp_X]/mLSchoenocaulon officinale seed — 6 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSolidago canadensis pollen — 12 [hp_X]/mLTaraxacum officinale pollen — 12 [hp_X]/mLTrifolium pratense pollen — 12 [hp_X]/mLXanthium strumarium pollen — 12 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- NaturalCareNDC labeler code 70163
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Pollen (Chemical structure)Vegetable Proteins (Chemical structure)
- Identifiers
- Product ID 70163-0031_fb763cfa-bd62-4a73-9732-24d04124158aSPL ID fb763cfa-bd62-4a73-9732-24d04124158aSPL set ID 00665933-176e-4f16-b6ee-b55217b8abb3UNII YKH834O4BH, 492225Q21H, 9W34L2CQ9A, 3029988O2T, ANT994T71D, 2HU33I03UY, 85Z8OHV3K7, 098LKX5NCN, C9642I91WL, 3POA0Q644U, G515RAI9FY, 65M88RW2EG, V825XJG64G, 6NAF1689IO, ETJ7Z6XBU4, 644CZ16IR5, WQ3S5294XY, 3SNK70F46Y, 2QOF601J1MUPC 0371400701010
- Pharmacologic class
- Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Pollen Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470163003102followed by a unit qualifier and the quantityPackage 70163-0031-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
USES: May help temporarily relieve allergy symptoms ■ runny nose ■ congestion ■ headache ■ itchy, watery eyes, ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.
About NDC 70163-0031
- What is NDC 70163-0031?
- 70163-0031 is the product NDC for Pollen Hayfever, Epinephrine 6 [hp_X]/mL + 18 more ingredients liquid, listed with the FDA by NaturalCare. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pollen Hayfever (Adrenalinum, Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Iodatum, Mugwort Pollen (Artemisia Vulgaris), Bellis Perennis, Brassica SPP, Chenopodium Album, Euphrasia Officinalis, Histaminum Hydrochloricum, Alfalfa Pollen (Medicago Sativa), Phleum Pratense, Yellow Dock Pollen (Rumex Crispus), Sabadilla, Silicea, Goldenrod Pollen (Solidago Canadensis), Dandelion Pollen (Taraxacum Officinale), Red Clover Pollen (Trifolium Pratense), Xanthium Strumarium).
- What is the active ingredient?
- Epinephrine, Onion, Ambrosia artemisiifolia whole, Arsenic triiodide, Artemisia vulgaris pollen, Bellis perennis whole, Brassica rapa subsp. Oleifera pollen, Chenopodium album pollen, Euphrasia stricta, Histamine dihydrochloride, Medicago sativa pollen, Phleum pratense pollen, Rumex crispus pollen, Schoenocaulon officinale seed, Silicon dioxide, Solidago canadensis pollen, Taraxacum officinale pollen, Trifolium pratense pollen, Xanthium strumarium pollen.
- Who is the labeler?
- NaturalCare, NDC labeler code 70163. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pollen Hayfever?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.