Coldcalm NDC 0220-9057

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9057Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9057Add 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
0220-9057-07	00220905707	1 POUCH in 1 PACKAGE (0220-9057-07) / 5 LIQUID in 1 POUCHMarketed from May 1, 2017
0220-9057-09	00220905709	1 POUCH in 1 PACKAGE (0220-9057-09) / 30 LIQUID in 1 POUCHMarketed from May 1, 2017
0220-9057-47	00220905747	1 POUCH in 1 PACKAGE (0220-9057-47) / 40 LIQUID in 1 POUCHMarketed from Sep 13, 2023

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, eupatorium perfoliatum flowering top, gelsemium sempervirens root, potassium dichromate, strychnos nux-vomica seed, phytolacca americana root, pulsatilla vulgaris
Active ingredients: Onion — 3 [hp_C]/1Apis mellifera — 15 [hp_C]/1Eupatorium perfoliatum flowering top — 3 [hp_C]/1Gelsemium sempervirens root — 6 [hp_C]/1Potassium dichromate — 6 [hp_C]/1Strychnos nux-vomica seed — 3 [hp_C]/1Phytolacca americana root — 6 [hp_C]/1Pulsatilla vulgaris — 6 [hp_C]/1
Dosage form: Liquid
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 1, 2017
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 0220-9057_3aad9396-ca5b-12a0-e063-6294a90a4b88SPL ID 3aad9396-ca5b-12a0-e063-6294a90a4b88SPL set ID 94afe9a0-2d11-11e7-818f-424c58303031UNII 492225Q21H, 7S82P3R43Z, 1W0775VX6E, 639KR60Q1Q, T4423S18FM, 269XH13919, 11E6VI8VEG, I76KB35JEVUPC 0306969057094
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

N400220905707 followed by a unit qualifier and the quantity

Package 00220-9057-07. 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 24, 2025.

Indications (excerpt from the label)

Uses* temporarily relieves cold symptoms such as: sneezing runny nose nasal congestion

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)