What is NDC 71753-1156?

71753-1156 is the product NDC for Cold Armor, Onion 6 [hp_X]/mL + 7 more ingredients spray, listed with the FDA by Ratis, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Cold Armor (Allium Cepa, Hydrastis Canadensis, Pulsatilla (Pratensis), Dulcamara, Nux Vomica, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum).

What is the active ingredient?

Onion, Goldenseal, Pulsatilla pratensis whole, Solanum dulcamara top, Strychnos nux-vomica seed, Ferrosoferric phosphate, Gelsemium sempervirens root, Potassium dichromate.

Ratis, LLC, NDC labeler code 71753. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cold Armor?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cold Armor NDC 71753-1156 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71753-1156Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71753-1156Add 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
71753-1156-1	7175311560171753115601	30 mL in 1 BOTTLE, SPRAY (71753-1156-1)Marketed from May 26, 2023

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): Cold Armor
Generic name (nonproprietary): allium cepa, hydrastis canadensis, pulsatilla (pratensis), dulcamara, nux vomica, ferrum phosphoricum, gelsemium sempervirens, kali bichromicum
Active ingredients: Onion — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLPulsatilla pratensis whole — 6 [hp_X]/mLSolanum dulcamara top — 8 [hp_X]/mLStrychnos nux-vomica seed — 8 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Ratis, LLCNDC labeler code 71753
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 26, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)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 IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 71753-1156_fb97f830-fce0-4a6d-81cf-ae5d2abe5de7SPL ID fb97f830-fce0-4a6d-81cf-ae5d2abe5de7SPL set ID 46af3f19-055e-4025-a14e-1d6c25880f4dUNII 492225Q21H, ZW3Z11D0JV, 8E272251DI, KPS1B1162N, 269XH13919, 91GQH8I5F7, 639KR60Q1Q, T4423S18FMUPC 0371753115618
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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

N471753115601 followed by a unit qualifier and the quantity

Package 71753-1156-01. 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 May 26, 2023.

Indications (excerpt from the label)

USES: May temporariy relieve stuffy and runny nose, coughing, congestion, body aches, fever, weakness, and minor sore throat.* * 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)

About NDC 71753-1156

What is NDC 71753-1156?: 71753-1156 is the product NDC for Cold Armor, Onion 6 [hp_X]/mL + 7 more ingredients spray, listed with the FDA by Ratis, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cold Armor (Allium Cepa, Hydrastis Canadensis, Pulsatilla (Pratensis), Dulcamara, Nux Vomica, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum).
What is the active ingredient?: Onion, Goldenseal, Pulsatilla pratensis whole, Solanum dulcamara top, Strychnos nux-vomica seed, Ferrosoferric phosphate, Gelsemium sempervirens root, Potassium dichromate.
Who is the labeler?: Ratis, LLC, NDC labeler code 71753. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cold Armor?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.