G05 Oxi-Met NDC 63479-0705

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0705Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0705Add 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
63479-0705-1	63479070501	30 mL in 1 BOTTLE, GLASS (63479-0705-1)Marketed from May 15, 1996

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): G05 Oxi-MetSuffix: OXI-MET
Generic name (nonproprietary): adenosine triphosphate, ignatia amara, kali phosphoricum, natrum muriaticum, nux vomica, sulphur
Active ingredients: Adenosine triphosphate — 5 [hp_X]/mLStrychnos ignatii seed — 2 [hp_Q]/mLDibasic potassium phosphate — 1 [hp_Q]/mLSodium chloride — 2 [hp_Q]/mLStrychnos nux-vomica seed — 1 [hp_Q]/mLSulfur — 7 [hp_C]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 15, 1996
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)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63479-0705_0e772402-6cf6-8c75-e063-6294a90a5c45SPL ID 0e772402-6cf6-8c75-e063-6294a90a5c45SPL set ID beb18213-911a-38d4-e053-2a95a90ac17cUNII 8L70Q75FXE, 1NM3M2487K, CI71S98N1Z, 451W47IQ8X, 269XH13919, 70FD1KFU70
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N463479070501 followed by a unit qualifier and the quantity

Package 63479-0705-01. 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

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