Amber Amethyst

UNIISPL

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

Identification

ManufacturerUriel Pharmacy, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895114085
60 g in 1 TUBE (48951-1408-5)

Annotations

UNII (FDA Substance ID)

70J9Z0J26P

AMBER

RxCUI 1311393

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "70J9Z0J26P",
    "rxcui": "1311393",
    "inchikey": null,
    "display_name": "AMBER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "4837e805-a777-c1fa-e063-6294a90ae9c4": {
      "match": "brand_token",
      "title": "AMBER AMETHYST OINTMENT [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2026-01-16"
    }
  },
  "productid": "48951-1408_4837e805-a778-c1fa-e063-6294a90ae9c4",
  "productndc": "48951-1408",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMBER; EQUISETUM ARVENSE WHOLE; HORSE CHESTNUT; SILICON DIOXIDE",
  "proprietary_name": "Amber Amethyst",
  "active_ingred_unit": "[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Amber Amethyst",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "3; 2; 2; 6"
}

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