S01 Allerdrain NDC 63479-1901

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-1901Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-1901Add 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
63479-1901-1	63479190101	30 mL in 1 BOTTLE, GLASS (63479-1901-1)Marketed from Mar 15, 1993

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): S01 AllerdrainSuffix: ALLERDRAIN
Generic name (nonproprietary): aloe socotrina, berberis vulgaris, betula verrucosa, bryonia, carduus marianus, echinacea angustifolia, ginkgo biloba, histaminum hydrochloricum, juniperus communis, lycopodium clavatum, melaleuca alternifolia oil, quercus robur, rhamnus purshiana, ribes nigrum, rosa canina, rosmarinus officinalis, scrophularia nodosa, senna, solidago virgaurea, taraxacum officinale, vaccinium vitus idaea
Active ingredients: Lycopodium clavatum spore — 4 [hp_X]/mLFrangula purshiana bark — 1 [hp_X]/mLQuercus robur flower bud — 2 [hp_X]/mLRibes nigrum flower bud — 2 [hp_X]/mLRosa canina leaf — 2 [hp_X]/mLScrophularia nodosa — 2 [hp_X]/mLMilk thistle — 2 [hp_X]/mLGinkgo — 2 [hp_X]/mLHistamine dihydrochloride — 200 [hp_X]/mLTea tree oil — 12 [hp_X]/mLRosmarinus officinalis flowering top — 2 [hp_X]/mLBerberis vulgaris root bark — 1 [hp_X]/mLBetula pendula leaf — 2 [hp_X]/mLBryonia alba root — 1 [hp_X]/mLAloe — 3 [hp_X]/mLJuniperus communis stem — 2 [hp_X]/mLVaccinium vitis-idaea leaf — 2 [hp_X]/mLEchinacea angustifolia — 2 [hp_X]/mLTaraxacum officinale — 2 [hp_X]/mLSenna leaf — 2 [hp_X]/mLSolidago virgaurea flowering top — 1 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 1993
Listing expires: Dec 31, 2026
Identifiers: Product ID 63479-1901_0e775a95-3ba3-f934-e063-6394a90a314fSPL ID 0e775a95-3ba3-f934-e063-6394a90a314fSPL set ID b9d2a7ef-28bd-4882-e053-2a95a90a0fddUNII C88X29Y479, 4VBP01X99F, VC5I578BE3, VYH9Y9BCCP, J3N2Z889QP, 7H443NUB2T, U946SH95EE, 19FUJ2C58T, 3POA0Q644U, VIF565UC2G, 8JM482TI79, 1TH8Q20J0U, 5HW39H9KDH, T7J046YI2B, V5VD430YW9, HBU87MH6OY, FO2ACM0RMQ, VB06AV5US8, 39981FM375, AK7JF626KX, 5405K23S50UPC 0818960012076

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

N463479190101 followed by a unit qualifier and the quantity

Package 63479-1901-01. 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 Jan 8, 2024.

Indications (excerpt from the label)

Uses: For temporary relief of minor: congestion* rashes* digestive discomfort* tiredness* flatulence* acne* *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)