Outdoor Allergies NDC 70163-0007

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0007Add 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
70163-0007-1	70163000701	1 BLISTER PACK in 1 CARTON (70163-0007-1) / 60 TABLET in 1 BLISTER PACKMarketed from Feb 23, 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): Outdoor Allergies
Generic name (nonproprietary): aconitum napellus, adrenalinum, allium cepa, ragweed pollen, arsenicum iodatum, mugwort pollen, mustard pollen, lambs quarters pollen, euphrasia officinalis, histaminum hydrochloricum, perennial rye grass pollen, alfalfa pollen, timothy grass pollen, yellow dock pollen, sabadilla, silicea, dandelion pollen, red clover pollen, cocklebur pollen
Active ingredients: Aconitum napellus whole — 6 [hp_X]/1Epinephrine — 6 [hp_X]/1Onion — 6 [hp_X]/1Ambrosia artemisiifolia whole — 12 [hp_X]/1Arsenic triiodide — 6 [hp_X]/1Artemisia vulgaris pollen — 12 [hp_X]/1Brassica rapa subsp. Oleifera pollen — 12 [hp_X]/1Chenopodium album pollen — 12 [hp_X]/1Euphrasia stricta — 6 [hp_X]/1Histamine dihydrochloride — 12 [hp_X]/1Lolium perenne pollen — 12 [hp_X]/1Medicago sativa pollen — 12 [hp_X]/1Phleum pratense pollen — 12 [hp_X]/1Rumex crispus pollen — 12 [hp_X]/1Schoenocaulon officinale seed — 6 [hp_X]/1Silicon dioxide — 6 [hp_X]/1Taraxacum officinale pollen — 12 [hp_X]/1Trifolium pratense pollen — 12 [hp_X]/1Xanthium strumarium pollen — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: NaturalCare
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 23, 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 70163-0007_01216112-fffe-45f1-a02f-28eac39c1c69SPL ID 01216112-fffe-45f1-a02f-28eac39c1c69SPL set ID b0a76faa-a081-4cee-ae40-e5605458bec3UNII U0NQ8555JD, YKH834O4BH, 492225Q21H, 9W34L2CQ9A, 3029988O2T, ANT994T71D, 85Z8OHV3K7, 098LKX5NCN, C9642I91WL, 3POA0Q644U, 4T81LB52R0, G515RAI9FY, 65M88RW2EG, V825XJG64G, 6NAF1689IO, ETJ7Z6XBU4, WQ3S5294XY, 3SNK70F46Y, 2QOF601J1M
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Pollen Allergenic Extract; 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

N470163000701 followed by a unit qualifier and the quantity

Package 70163-0007-01. 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 Feb 23, 2026.

Indications (excerpt from the label)

USES: May help temporarily relieve allergy symptoms ■ runny nose ■ congestion ■ headache ■ sore throat ■ sneezing ■ itchy, watery eyes* *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)