Terebinthina

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766216271
200 PELLET in 1 VIAL, GLASS (37662-1627-1)
ndc11
3766216272
500 PELLET in 1 VIAL, GLASS (37662-1627-2)
ndc11
3766216273
3000 PELLET in 1 BOTTLE, GLASS (37662-1627-3)
ndc11
3766216274
10000 PELLET in 1 BOTTLE, GLASS (37662-1627-4)

Annotations

UNII (FDA Substance ID)

C5H0QJ6V7F

TURPENTINE OIL

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C5H0QJ6V7F",
    "rxcui": null,
    "inchikey": null,
    "display_name": "TURPENTINE OIL",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1363fff1-3b37-47d8-a17b-8bf8e72f6616": {
      "match": "brand_token",
      "title": "TEREBINTHINA COMBINATION 9248 (TEREBINTHINA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1627_e9c4851b-1216-3272-e053-2995a90a64a3",
  "productndc": "37662-1627",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TURPENTINE OIL",
  "proprietary_name": "Terebinthina",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Terebinthina",
  "start_marketing_date": "20220928",
  "active_numerator_strength": "500"
}

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