Vicks DayQuil and Vicks NyQuil

SPL

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

Identification

ManufacturerThe Procter & Gamble Manufacturing Company

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3700004524
1 KIT in 1 PACKAGE (37000-045-24) * 354 mL in 1 BOTTLE, PLASTIC (37000-810-12) * 354 mL in 1 BOTTLE, PLASTIC (37000-815-12)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": null,
  "spl_meta": {
    "526cdb40-aa65-4885-e063-6294a90afa0c": {
      "match": "brand_token",
      "title": "VICKS VAPOFREEZE PAIN RELIEF (CAMPHOR, MENTHOL) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]",
      "spl_version": "1",
      "published_date": "2026-05-25"
    }
  },
  "productid": "37000-045_4b44cda7-efb4-ef0b-e063-6294a90aba1c",
  "productndc": "37000-045",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": null,
  "proprietary_name": "Vicks DayQuil and Vicks NyQuil",
  "active_ingred_unit": null,
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and doxylamine succinate",
  "start_marketing_date": "20140731",
  "active_numerator_strength": null
}

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