Ultra Strength Pain Relief Gel

SPL

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

Identification

ManufacturerTELEBRANDS CORP

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7328702301
1 APPLICATOR in 1 CARTON (73287-023-01) / 71 g in 1 APPLICATOR

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "73287-023_275b89dc-566d-3bc1-e063-6394a90a9cad",
  "productndc": "73287-023",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "Ultra Strength Pain Relief Gel",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20220228",
  "active_numerator_strength": "8"
}

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