Ultra concentrated Daytime/ Nighttime Severe Softgel

SPL

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

Identification

ManufacturerCVS PHARMACY, INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5131654724
2 BLISTER PACK in 1 CARTON (51316-547-24) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK * 4 CAPSULE in 1 BLISTER PACK

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "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": "51316-547_4de9aabc-fafa-fd37-e063-6294a90ab10c",
  "productndc": "51316-547",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": null,
  "proprietary_name": "Ultra concentrated Daytime/ Nighttime Severe Softgel",
  "active_ingred_unit": null,
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine hydrochloride softgel",
  "start_marketing_date": "20250201",
  "active_numerator_strength": null
}

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