R13 Adrenal NDC 63479-1813

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-1813Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-1813Add 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
63479-1813-1	63479181301	30 mL in 1 BOTTLE, GLASS (63479-1813-1)Marketed from Nov 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): R13 AdrenalSuffix: ADRENAL
Generic name (nonproprietary): activated charcoal, causticum, arabica coffee bean, prasterone, glycyrrhiza glabra, ribes nigrum flower bud, eleuthero, and veratrum album root
Active ingredients: Activated charcoal — 7 [hp_C]/mLCausticum — 1 [hp_Q]/mLArabica coffee bean — 7 [hp_C]/mLPrasterone — 3 [hp_Q]/mLGlycyrrhiza glabra — 6 [hp_C]/mLRibes nigrum flower bud — 1 [hp_X]/mLEleuthero — 1 [hp_C]/mLVeratrum album root — 7 [hp_C]/mL
Dosage form: Solution
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
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63479-1813_0e77566d-437a-c560-e063-6294a90ae164SPL ID 0e77566d-437a-c560-e063-6294a90ae164SPL set ID 82bfbb2f-8487-4eda-8454-3cbb5d40bc76UNII 2P3VWU3H10, DD5FO1WKFU, 3SW678MX72, 459AG36T1B, 2788Z9758H, VYH9Y9BCCP, ZQH6VH092Z, QNS6W5US1ZUPC 0818960012762
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479181301 followed by a unit qualifier and the quantity

Package 63479-1813-01. 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: fatigue* stress* muscle weakness* dizziness when standing* hives* salt cravings* *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)