Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Dry Eczema Drops 2006 (Dry eczema drops) NDC 63083-2006
Clematis recta flowering top 4 [hp_X]/59mL + 4 more ingredients · Liquid · Oral · Professional Complementary Health Formulas
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63083-2006-2 | 6308320060263083200602 | 59 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
N463083200602followed by a unit qualifier and the quantityPackage 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.
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.