Tucks Medicated Cooling Pads

UNIISPL

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

Identification

ManufacturerBlistex Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
1015721031
1 JAR in 1 CARTON (10157-2103-1) / 40 APPLICATOR in 1 JAR / 1 mL in 1 APPLICATOR
ndc11
1015721032
1 JAR in 1 CARTON (10157-2103-2) / 100 APPLICATOR in 1 JAR / 1 mL in 1 APPLICATOR
ndc11
1015721033
40 APPLICATOR in 1 JAR (10157-2103-3) / 1 mL in 1 APPLICATOR
ndc11
1015721034
2 JAR in 1 CARTON (10157-2103-4) / 100 APPLICATOR in 1 JAR / 1 mL in 1 APPLICATOR

Annotations

UNII (FDA Substance ID)

101I4J0U34

WITCH HAZEL

RxCUI 89821

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "101I4J0U34",
    "rxcui": "89821",
    "inchikey": null,
    "display_name": "WITCH HAZEL",
    "substance_type": "structurallyDiverse",
    "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": "10157-2103_7b87eeff-5bf9-4f03-b38a-5d7557ce49bf",
  "productndc": "10157-2103",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "Tucks Medicated Cooling Pads",
  "active_ingred_unit": "mg/mL",
  "application_number": "M015",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "WITCH HAZEL",
  "start_marketing_date": "20160830",
  "active_numerator_strength": "500"
}

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