Hydrate II NDC 81825-0001

NDC codes

FDA NDC Directory

Product NDC (as listed)81825-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width81825-0001Add 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
81825-0001-2	81825000102	60 mL in 1 BOTTLE, DROPPER (81825-0001-2)Marketed from Feb 16, 2022

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): Hydrate II
Generic name (nonproprietary): berber aqui, beta vulg, boldo, carduus mar, chelidonium maj, hordeum vulgare, iris vers, rosmarinus, taraxacum, avena, eleutherococcus senticosus, xanthoxylum, equisetum hyem, hypericum, ulmus fulv, gettysburg aqua, glycyrrhiza, wildbad aqua, carlsbad aqua, atp, hydrogen, nat mur, oxygen, silicea, wiesbaden aqua
Active ingredients: Berberis aquifolium root bark — 8 [hp_X]/mLBeta vulgaris whole — 8 [hp_X]/mLPeumus boldus leaf — 8 [hp_X]/mLMilk thistle — 8 [hp_X]/mLChelidonium majus whole — 8 [hp_X]/mLHordeum vulgare whole — 8 [hp_X]/mLIris versicolor root — 8 [hp_X]/mLSalvia rosmarinus flowering top — 8 [hp_X]/mLTaraxacum officinale — 8 [hp_X]/mLAvena sativa flowering top — 8 [hp_X]/mLEleutherococcus senticosus whole — 8 [hp_X]/mLZanthoxylum americanum bark — 8 [hp_X]/mLEquisetum hyemale whole — 8 [hp_X]/mLHypericum perforatum whole — 8 [hp_X]/mLUlmus rubra bark — 8 [hp_X]/mLGlycyrrhiza glabra — 12 [hp_X]/mLAdenosine triphosphate — 30 [hp_C]/mLHydrogen — 34 [hp_C]/mLSodium chloride — 30 [hp_C]/mLOxygen — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Zorex International
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 16, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 81825-0001_bcaaa148-5549-4a13-b358-47bd4354a316SPL ID bcaaa148-5549-4a13-b358-47bd4354a316SPL set ID e5f53495-3b75-4d7c-89af-23058fb6fd05UNII VZJ9F3C3SB, 4G174V5051, Q4EWM09M3O, U946SH95EE, 7E889U5RNN, 8JBE478M5Q, X43D4L3DQC, 8JM482TI79, 39981FM375, MA9CQJ3F7F, ZX5Z2LW23O, A4KL1HMZ7T, 59677RXH25, XK4IUX8MNB, 91QY4PXU8Q, 2788Z9758H, 8L70Q75FXE, 7YNJ3PO35Z, 451W47IQ8X, S88TT14065, ETJ7Z6XBU4UPC 0713289147792
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

N481825000102 followed by a unit qualifier and the quantity

Package 81825-0001-02. 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 low energy, circulatory disorders, digestive upset, &/or symptoms related to poor cellular hydration.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)