Cold and Flu Maximum Strength NDC 51393-5000

NDC codes

FDA NDC Directory

Product NDC (as listed)51393-5000Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51393-5000Add 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
51393-5000-1	51393500001	1 BOTTLE, DISPENSING in 1 CARTON (51393-5000-1) / 10 mL in 1 BOTTLE, DISPENSINGMarketed from Feb 1, 2019
51393-5000-3	51393500003	1 BOTTLE, DISPENSING in 1 CARTON (51393-5000-3) / 30 mL in 1 BOTTLE, DISPENSINGMarketed from Oct 15, 2021

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 and Flu Maximum StrengthSuffix: Maximum Strength
Generic name (nonproprietary): european elderberry, berberis vulgaris root, solidago canadensis flowering top, achillea millefolium flowering top, holy basil leaf, garlic, ginger, and fenugreek seed
Active ingredients: European elderberry — 89 [hp_C]/100mLBerberis vulgaris root — 34 [hp_C]/100mLSolidago canadensis flowering top — 21 [hp_C]/100mLAchillea millefolium flowering top — 8 [hp_C]/100mLHoly basil leaf — 89 [hp_C]/100mLGarlic — 89 [hp_C]/100mLGinger — 89 [hp_C]/100mLFenugreek seed — 89 [hp_C]/100mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Forces of Nature
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 2019
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)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)
Identifiers: Product ID 51393-5000_57e009f1-f90c-c1f0-e063-6394a90ad048SPL ID 57e009f1-f90c-c1f0-e063-6394a90ad048SPL set ID f46dbd8c-a9c0-4069-94dc-4c700dda8643UNII BQY1UBX046, ITJ40JX79U, ZHL562L3PR, 55862Q3XEU, SCJ765569P, V1V998DC17, C5529G5JPQ, 654825W09Z
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451393500001 followed by a unit qualifier and the quantity

Package 51393-5000-01. 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 Jul 30, 2026.

Indications (excerpt from the label)

Uses For the temporary relief of respiratory ailments (cold & flu). Symptoms including: Cough Body Aches Fever Nasal Congestion Respiratory Issues Sinus Pressure

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)