Benzoin Tincture

UNIISPL

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

Identification

ManufacturerPharma Nobis, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8264592492
59 mL in 1 BOTTLE, PLASTIC (82645-924-92)

Annotations

UNII (FDA Substance ID)

GK21SBA74R

BENZOIN RESIN

RxCUI 1406

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "GK21SBA74R",
    "rxcui": "1406",
    "inchikey": null,
    "display_name": "BENZOIN RESIN",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "a893a232-2ea8-4e0d-8cbf-7f5040b3be2e": {
      "match": "brand_token",
      "title": "BENZOIN COMPOUND TINCTURE (BENZOIN RESIN) LIQUID [HUMCO HOLDING GROUP, INC.]",
      "spl_version": "7",
      "published_date": "2025-12-12"
    }
  },
  "productid": "82645-924_0d6cc91d-1d9b-25ae-e063-6394a90aa6a0",
  "productndc": "82645-924",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZOIN RESIN",
  "proprietary_name": "Benzoin Tincture",
  "active_ingred_unit": "mg/mL",
  "application_number": "M022",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzoin Resin",
  "start_marketing_date": "20080101",
  "active_numerator_strength": "1000"
}

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