Muscle Freeze Relief

UNIISPL

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

Identification

ManufacturerNATURAL ESSENTIALS, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
6690241003
85 g in 1 CONTAINER (66902-410-03)
ndc11
6690241004
113 g in 1 BOTTLE (66902-410-04)
ndc11
6690241015
425 g in 1 BOTTLE (66902-410-15)
ndc11
6690241016
453 g in 1 BOTTLE (66902-410-16)
ndc11
6690241028
3629 g in 1 JUG (66902-410-28)
ndc11
6690241055
195498 g in 1 DRUM (66902-410-55)

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": {
    "163ba925-b26a-4737-8c05-68875435452b": {
      "match": "brand_token",
      "title": "MUSCLE RUB (MENTHOL, METHYL SALICYLATE) CREAM [ALDERMED INC.]",
      "spl_version": "5",
      "published_date": "2026-05-11"
    }
  },
  "productid": "66902-410_240d1402-4d06-62ff-e063-6294a90ad60c",
  "productndc": "66902-410",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Muscle Freeze Relief",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20210715",
  "active_numerator_strength": "37"
}

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