Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On

UNIISPL

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

Identification

ManufacturerTARGET CORPORATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1167326103
89 mL in 1 BOTTLE, WITH APPLICATOR (11673-261-03)

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": {
    "51c9bdee-dcff-2818-e063-6294a90abb47": {
      "match": "brand_token",
      "title": "TARGET UP AND UP SPF 30 DEEP REPAIR FACIAL MOISTURIZER SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [TARGET CORPORATION]",
      "spl_version": "1",
      "published_date": "2026-05-20"
    }
  },
  "productid": "11673-261_0f95e27d-e2be-917a-e063-6294a90a5709",
  "productndc": "11673-261",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20231121",
  "active_numerator_strength": "40"
}

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