Coldcalm NDC 0220-9048

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9048Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9048Add 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
0220-9048-04	00220904804	60 TABLET in 1 BLISTER PACK (0220-9048-04)Marketed from Jan 1, 1995
0220-9048-29	00220904829	120 TABLET in 1 BLISTER PACK (0220-9048-29)Marketed from Dec 9, 2020
0220-9048-91	00220904891	20 TABLET in 1 BLISTER PACK (0220-9048-91)Marketed from Jul 14, 2021
0220-9048-92	00220904892	100 TABLET in 1 BLISTER PACK (0220-9048-92)Marketed from Apr 1, 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): Coldcalm
Generic name (nonproprietary): onion, apis mellifera, atropa belladonna, eupatorium perfoliatum flowering top, gelsemium sempervirens root, strychnos nux-vomica seed, phytolacca americana root, pulsatilla vulgaris, dichromate ion
Active ingredients: Onion — 3 [hp_C]/1Apis mellifera — 6 [hp_C]/1Atropa belladonna — 6 [hp_C]/1Eupatorium perfoliatum flowering top — 3 [hp_C]/1Gelsemium sempervirens root — 6 [hp_C]/1Dichromate ion — 6 [hp_C]/1Strychnos nux-vomica seed — 3 [hp_C]/1Phytolacca americana root — 6 [hp_C]/1Pulsatilla vulgaris — 6 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1995
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)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 IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 0220-9048_31bbb16b-e155-90c4-e063-6394a90af542SPL ID 31bbb16b-e155-90c4-e063-6394a90af542SPL set ID af4a4765-8255-44fb-821c-4345a2a45e2aUNII 492225Q21H, 7S82P3R43Z, WQZ3G9PF0H, 1W0775VX6E, 639KR60Q1Q, 9LKY4BFN2V, 269XH13919, 11E6VI8VEG, I76KB35JEV
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom 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

N400220904804 followed by a unit qualifier and the quantity

Package 00220-9048-04. 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 Apr 1, 2025.

Indications (excerpt from the label)

Uses* temporarily relieves cold symptoms such as: sneezing runny nose nasal congestion occasional minor sore throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)