AllergyCalm NDC 0220-9306

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9306Add 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
0220-9306-04	00220930604	3 BLISTER PACK in 1 BOX (0220-9306-04) / 20 TABLET in 1 BLISTER PACKMarketed from Mar 1, 2022
0220-9306-29	00220930629	6 BLISTER PACK in 1 BOX (0220-9306-29) / 20 TABLET in 1 BLISTER PACKMarketed from Aug 1, 2022
0220-9306-91	00220930691	1 BLISTER PACK in 1 BOX (0220-9306-91) / 20 TABLET in 1 BLISTER PACKMarketed from Jun 6, 2023
0220-9306-92	00220930692	5 BLISTER PACK in 1 BOX (0220-9306-92) / 20 TABLET in 1 BLISTER PACKMarketed from Apr 15, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): AllergyCalm
Generic name (nonproprietary): onion, ambrosia artemisiifolia, euphrasia stricta, histamine dihydrochloride, schoenocaulon officinale seed, solidago virgaurea flowering top
Active ingredients: Schoenocaulon officinale seed — 5 [hp_C]/1Histamine dihydrochloride — 9 [hp_C]/1Euphrasia stricta — 5 [hp_C]/1Ambrosia artemisiifolia — 5 [hp_C]/1Solidago virgaurea flowering top — 5 [hp_C]/1Onion — 5 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 1, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 0220-9306_38e22593-4061-ae63-e063-6294a90a3d39SPL ID 38e22593-4061-ae63-e063-6294a90a3d39SPL set ID d92d9269-7532-2f0e-e053-2a95a90ab0d6UNII 6NAF1689IO, 3POA0Q644U, C9642I91WL, 9W34L2CQ9A, 5405K23S50, 492225Q21H
Pharmacologic class: Non-Standardized Food Allergenic Extract

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

N400220930604 followed by a unit qualifier and the quantity

Package 00220-9306-04. 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 Jul 1, 2025.

Indications (excerpt from the label)

Uses* temporarily relieves these symptoms of hay fever or other upper respiratory allergies: ▪ itchy and watery eyes ▪ sneezing ▪ itchy throat and nose ▪ runny nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)