Pollen Hayfever NDC 70163-0031

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0031Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0031Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70163-0031-2	70163003102	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: NaturalCare
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 5, 2026
Listing expires: Dec 31, 2027
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

N470163003102 followed by a unit qualifier and the quantity

Package 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 May 5, 2026.

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.

Full label on DailyMed (opens in a new tab)