Meijer Maximum Strength Pain Relieving

UNIISPL

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

Identification

ManufacturerMeijer Distribution, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4125035001
1 BOTTLE, WITH APPLICATOR in 1 CARTON (41250-350-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR

Annotations

UNII (FDA Substance ID)

L7T10EIP3A

MENTHOL, UNSPECIFIED FORM

RxCUI 6750

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "L7T10EIP3A",
    "rxcui": "6750",
    "inchikey": null,
    "display_name": "MENTHOL, UNSPECIFIED FORM",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "a5f7bd55-55c3-4b0e-a16c-33bbea40536a": {
      "match": "brand_token",
      "title": "MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE) LIQUID [MEIJER DISTRIBUTION INC.]",
      "spl_version": "5",
      "published_date": "2026-06-01"
    }
  },
  "productid": "41250-350_2c052527-8626-4799-8c2c-1ebaa310890c",
  "productndc": "41250-350",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Meijer Maximum Strength Pain Relieving",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "menthol, unspecified form",
  "start_marketing_date": "20190224",
  "active_numerator_strength": "160"
}

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