24 7 Relief and Recovery Pain Relieving

UNIISPL

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

Identification

ManufacturerTriplicare Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
8765696404
118 mL in 1 TUBE (87656-964-04)
ndc11
8765696432
946 mL in 1 BOTTLE (87656-964-32)

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": {
    "53ca807b-3ec2-4b5e-aa5a-6dcb756bb423": {
      "match": "brand_token",
      "title": "24 7 RELIEF AND RECOVERY PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) CREAM [TRIPLICARE INC]",
      "spl_version": "1",
      "published_date": "2026-05-06"
    }
  },
  "productid": "87656-964_50acffaf-7b87-df5e-e063-6394a90ad6b5",
  "productndc": "87656-964",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "24 7 Relief and Recovery Pain Relieving",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, UNSPECIFIED FORM",
  "start_marketing_date": "20260413",
  "active_numerator_strength": "37"
}

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