NDC codes

FDA NDC Directory
Product NDC (as listed)63083-2006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-2006Add 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
63083-2006-2630832006026308320060259 mL in 1 BOTTLE, DROPPER (63083-2006-2)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)
Dry Eczema Drops 2006Suffix: 2006
Generic name (nonproprietary)
dry eczema drops
Active ingredients
Clematis recta flowering top — 4 [hp_X]/59mLPotassium sulfate — 6 [hp_X]/59mLCalcium sulfide — 8 [hp_X]/59mLGraphite — 12 [hp_X]/59mLOyster shell calcium carbonate, Crude — 30 [hp_X]/59mL
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
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers
Product ID 63083-2006_ad4d42f3-6735-435c-8be0-e284f9a9d0a0SPL ID ad4d42f3-6735-435c-8be0-e284f9a9d0a0SPL set ID 72e775e7-e5fb-40fc-a96a-bc1b6015cc93UNII 396421SP9F, 1K573LC5TV, 1MBW07J51Q, 4QQN74LH4O, 2E32821G6I
Pharmacologic class
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083200602 followed by a unit qualifier and the quantity

Package 63083-2006-02. 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 .

Indications (excerpt from the label)

INDICATIONS For the temporary relief of dry, irritated, red, or itchy skin.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2006

What is NDC 63083-2006?
63083-2006 is the product NDC for Dry Eczema Drops 2006 (dry eczema drops), Clematis recta flowering top 4 [hp_X]/59mL + 4 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?
Dry Eczema Drops 2006 (Dry Eczema Drops).
What is the active ingredient?
Clematis recta flowering top, Potassium sulfate, Calcium sulfide, Graphite, Oyster shell calcium carbonate, Crude.
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 Dry Eczema Drops 2006?
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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