Wet Eczema Drops 2136 (wet eczema drops) NDC 63083-2136

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2136Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2136Add 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
63083-2136-2	63083213602	59 mL in 1 BOTTLE, DROPPER (63083-2136-2)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): Wet Eczema Drops 2136Suffix: 2136
Generic name (nonproprietary): wet eczema drops
Active ingredients: Arsenic triiodide — 6 [hp_X]/59mLOyster shell calcium carbonate, Crude — 6 [hp_X]/59mLClematis recta flowering top — 6 [hp_X]/59mLCalcium sulfide — 6 [hp_X]/59mLPotassium sulfate — 6 [hp_X]/59mLDaphne mezereum bark — 6 [hp_X]/59mLLiquid petroleum — 6 [hp_X]/59mLToxicodendron pubescens leaf — 6 [hp_X]/59mLSulfur — 8 [hp_X]/59mLArsenic trioxide — 9 [hp_X]/59mLGraphite — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
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 63083-2136_0597f5dc-11b0-423c-b516-3fea39591f30SPL ID 0597f5dc-11b0-423c-b516-3fea39591f30SPL set ID 28f08a29-9b1a-4579-a56f-4cab7cdcfcb6UNII 3029988O2T, 2E32821G6I, 396421SP9F, 1MBW07J51Q, 1K573LC5TV, X2N6E405GV, 6ZAE7X688J, 6IO182RP7A, 70FD1KFU70, S7V92P67HO, 4QQN74LH4O
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

N463083213602 followed by a unit qualifier and the quantity

Package 63083-2136-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)