What is NDC 63083-1013?

63083-1013 is the product NDC for Poison Ivy/Oak 1013 (poison ivy/oak), Echinacea purpurea whole 2 [hp_X]/59mL + 11 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?

Poison Ivy/Oak 1013 (Poison Ivy/Oak).

What is the active ingredient?

Echinacea purpurea whole, Sus scrofa adrenal gland, Corticotropin, Beef liver, Croton tiglium seed, Histamine dihydrochloride, Wood creosote, Xerophyllum asphodeloides whole, Toxicodendron diversilobum leaf, Toxicodendron pubescens leaf, Urtica dioica subsp. Dioica leaf, Ailanthus altissima fruit.

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 Poison Ivy/Oak 1013?

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.

Poison Ivy/Oak 1013 NDC 63083-1013

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-1013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-1013Add 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
63083-1013-2	6308310130263083101302	59 mL in 1 BOTTLE, DROPPER (63083-1013-2)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): Poison Ivy/Oak 1013Suffix: 1013
Generic name (nonproprietary): poison ivy/oak
Active ingredients: Echinacea purpurea whole — 2 [hp_X]/59mLSus scrofa adrenal gland — 6 [hp_X]/59mLCorticotropin — 6 [hp_X]/59mLBeef liver — 6 [hp_X]/59mLCroton tiglium seed — 8 [hp_X]/59mLHistamine dihydrochloride — 12 [hp_X]/59mLWood creosote — 12 [hp_X]/59mLXerophyllum asphodeloides whole — 12 [hp_X]/59mLToxicodendron diversilobum leaf — 6 [hp_X]/59mLToxicodendron pubescens leaf — 6 [hp_X]/59mLUrtica dioica subsp. Dioica leaf — 6 [hp_X]/59mLAilanthus altissima fruit — 6 [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: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Adrenocorticotropic Hormone (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Meat Proteins (EXT)
Identifiers: Product ID 63083-1013_885f50d0-117a-4b26-8394-2464c173d389SPL ID 885f50d0-117a-4b26-8394-2464c173d389SPL set ID a75d1f82-703b-48a3-a6a2-a7ed1cdde0afUNII QI7G114Y98, 398IYQ16YV, K0U68Q2TXA, W8N8R55022, 0HK2GZK66E, 3POA0Q644U, 3JYG22FD73, 9I4XB1GP2B, V727AWD6ZZ, 6IO182RP7A, 232L6DS3Y4, 0W913N2K5N
Pharmacologic class: Adrenocorticotropic Hormone; Non-Standardized Food 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083101302 followed by a unit qualifier and the quantity

Package 63083-1013-02. 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 redness, swelling, stinging, itching of skin, and itching of nose or throat due to sensitivity to poison ivy and poison oak.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-1013

What is NDC 63083-1013?: 63083-1013 is the product NDC for Poison Ivy/Oak 1013 (poison ivy/oak), Echinacea purpurea whole 2 [hp_X]/59mL + 11 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?: Poison Ivy/Oak 1013 (Poison Ivy/Oak).
What is the active ingredient?: Echinacea purpurea whole, Sus scrofa adrenal gland, Corticotropin, Beef liver, Croton tiglium seed, Histamine dihydrochloride, Wood creosote, Xerophyllum asphodeloides whole, Toxicodendron diversilobum leaf, Toxicodendron pubescens leaf, Urtica dioica subsp. Dioica leaf, Ailanthus altissima fruit.
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 Poison Ivy/Oak 1013?: 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.

Poison Ivy/Oak 1013 (Poison ivy/oak) NDC 63083-1013