Flora Plus NDC 61626-0108

NDC codes

FDA NDC Directory

Product NDC (as listed)61626-0108Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61626-0108Add 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
61626-0108-4	61626010804	59.1 mL in 1 BOTTLE (61626-0108-4)Marketed from Dec 4, 2018

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): Flora Plus
Generic name (nonproprietary): aloe, alumina, antimon crud, arg nit, chelidonium maj, gambogia, graphites, hydrastis, lycopodium, silicea
Active ingredients: Aloe vera leaf — 12 [hp_X]/59.1mLAluminum oxide — 12 [hp_X]/59.1mLAntimony trisulfide — 12 [hp_X]/59.1mLSilver nitrate — 12 [hp_X]/59.1mLChelidonium majus — 12 [hp_X]/59.1mLGamboge — 12 [hp_X]/59.1mLGraphite — 12 [hp_X]/59.1mLGoldenseal — 12 [hp_X]/59.1mLLycopodium clavatum spore — 12 [hp_X]/59.1mLSilicon dioxide — 12 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: NET Remedies
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 4, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 61626-0108_b96ae7f1-7d4e-a211-e053-2995a90ab6e2SPL ID b96ae7f1-7d4e-a211-e053-2995a90ab6e2SPL set ID fc1ced48-bd9f-4b3f-b786-573fba072975UNII ZY81Z83H0X, LMI26O6933, F79059A38U, 95IT3W8JZE, 7E889U5RNN, 7556HJ7587, 4QQN74LH4O, ZW3Z11D0JV, C88X29Y479, ETJ7Z6XBU4

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

N461626010804 followed by a unit qualifier and the quantity

Package 61626-0108-04. 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 Jan 21, 2021.

Indications (excerpt from the label)

INDICATIONS FOR USE: For temporary relief of bowel congestions-constipation, gas, bloating • Digestive disturbance and intestinal complaints from bread, acids, sour wines, fermentable foods-sweets-yeast • White or yellow film on tongue • Relief of symptoms associated with yeast infections • Sensitivity in lower right abdominal area. **

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)