NDC codes

FDA NDC Directory
Product NDC (as listed)63083-9308Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-9308Add 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 NDC11-digit (billing)PackageCopy
63083-9308-16308393080129.5 mL in 1 BOTTLE, DROPPER (63083-9308-1)Marketed from Aug 15, 1985

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)
Energy Regulation Combination 9308Suffix: 9308
Generic name (nonproprietary)
energy regulation combination
Active ingredients
Sodium carbonate — 3 [hp_X]/29.5mLPulsatilla montana whole — 6 [hp_X]/29.5mLCalcium sulfide — 10 [hp_X]/29.5mLSulfur — 10 [hp_X]/29.5mLCreatine — 12 [hp_X]/29.5mL3-hydroxy-1-methylguanine — 12 [hp_X]/29.5mL
Dosage form
Liquid
Route
Oral
Labeler
Professional Complementary Health FormulasNDC labeler code 63083
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 63083-9308_0bcb9edb-9c1f-45eb-8d8c-c0e0842b71b9SPL ID 0bcb9edb-9c1f-45eb-8d8c-c0e0842b71b9SPL set ID b091febb-f18f-46d1-8bb8-d911de4c8935UNII 45P3261C7T, 24K790T39B, 1MBW07J51Q, 70FD1KFU70, MU72812GK0, 01VNU8ZSO0

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

N463083930801 followed by a unit qualifier and the quantity

Package 63083-9308-01. 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 .

Indications (excerpt from the label)

INDICATIONS For the temporary relief of exhaustion, fatigue, or debility.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-9308

What is NDC 63083-9308?
63083-9308 is the product NDC for Energy Regulation Combination 9308, Sodium carbonate 3 [hp_X]/29.5mL + 5 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Energy Regulation Combination 9308 (Energy Regulation Combination).
What is the active ingredient?
Sodium carbonate, Pulsatilla montana whole, Calcium sulfide, Sulfur, Creatine, 3-hydroxy-1-methylguanine.
Who is the labeler?
Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Energy Regulation Combination 9308?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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