Pain Relieving Roll-On

UNIISPL

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

Identification

ManufacturerSafetec of America, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6101015501
88 mL in 1 BOTTLE (61010-1550-1)

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": {
    "bad8ac0a-518d-4639-9b92-a39e0d437238": {
      "match": "brand_token",
      "title": "PAIN AND FEVER CHEWABLES CHILDRENS (ACETAMINOPHEN) TABLET, CHEWABLE [CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED]",
      "spl_version": "2",
      "published_date": "2026-05-28"
    }
  },
  "productid": "61010-1550_10a91ff8-4d59-15dd-e063-6394a90a3aad",
  "productndc": "61010-1550",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Pain Relieving Roll-On",
  "active_ingred_unit": "g/100mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "menthol, unspecified form",
  "start_marketing_date": "20191007",
  "active_numerator_strength": "7"
}

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