E.N.V. NDC 81825-0003

NDC codes

FDA NDC Directory

Product NDC (as listed)81825-0003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width81825-0003Add 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
81825-0003-1	81825000301	30 mL in 1 BOTTLE, DROPPER (81825-0003-1)Marketed from Dec 8, 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): E.N.V.
Generic name (nonproprietary): belladonna, berberis vulg, carduus mar, chelidonium maj, colocynthis, dioscorea, hydrastis, lycopodium, nat sulphuricum, nux vom, phos, pulsatilla, veratrum alb
Active ingredients: Atropa belladonna — 30 [hp_C]/mLBerberis vulgaris root bark — 30 [hp_C]/mLMilk thistle — 30 [hp_C]/mLChelidonium majus whole — 30 [hp_C]/mLCitrullus colocynthis fruit pulp — 30 [hp_C]/mLDioscorea villosa tuber — 30 [hp_C]/mLGoldenseal — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSodium sulfate — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLPulsatilla vulgaris whole — 30 [hp_C]/mLVeratrum album root — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Zorex International
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 8, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 81825-0003_70783c3e-4437-477e-8a45-0345fbcf573aSPL ID 70783c3e-4437-477e-8a45-0345fbcf573aSPL set ID 838498ba-cab9-4e1b-a567-e7f1862b7fbbUNII WQZ3G9PF0H, 1TH8Q20J0U, U946SH95EE, 7E889U5RNN, 23H32AOH17, IWY3IWX2G8, ZW3Z11D0JV, C88X29Y479, 0YPR65R21J, 269XH13919, 27YLU75U4W, I76KB35JEV, QNS6W5US1ZUPC 0713289148126
Pharmacologic class: 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

N481825000301 followed by a unit qualifier and the quantity

Package 81825-0003-01. 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 Dec 21, 2018.

Indications (excerpt from the label)

USES: Temporarily relieves flatulence, constipation, and belching.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)