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United States · US · US:10157-2126_19acdb94-4437-4eaf-aa16-0bef186d9f8a

Tucks Triple Relief Hemorrhoidal

UNIISPLATC A06AG

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBlistex Inc.
CountryUS (United States)
ATC codeA06AG
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1015721261
    1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR

Annotations

UNII (FDA Substance ID)
PDC6A3C0OX
GLYCERIN
RxCUI 4910
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "PDC6A3C0OX",
    "rxcui": "4910",
    "inchikey": "PEDCQBHIVMGVHV-UHFFFAOYSA-N",
    "display_name": "GLYCERIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "bf892e90-2d9b-4fa0-8ee4-8a2736be6c30": {
      "match": "brand_token",
      "title": "TUCKS TRIPLE RELIEF HEMORRHOIDAL (WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE) CREAM [BLISTEX INC.]",
      "spl_version": "1",
      "published_date": "2025-01-08"
    }
  },
  "productid": "10157-2126_19acdb94-4437-4eaf-aa16-0bef186d9f8a",
  "productndc": "10157-2126",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GLYCERIN; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE; WHITE PETROLATUM",
  "proprietary_name": "Tucks Triple Relief Hemorrhoidal",
  "active_ingred_unit": "g/100g; g/100g; g/100g; g/100g",
  "application_number": "M015",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, and PHENYLEPHRINE HYDROCHLORIDE",
  "start_marketing_date": "20250106",
  "active_numerator_strength": "15; .25; 1; 16"
}

Related drugs

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