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United States · US · US:70000-0132_411c9eb3-fe39-f3db-e063-6394a90a82df

Extra Strength Sinus Relief Nasal Decongestant

UNIISPLATC R01AA04

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerCARDINAL HEALTH
CountryUS (United States)
ATC codeR01AA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7000001321
    1 BOTTLE, SPRAY in 1 CARTON (70000-0132-1) / 30 mL in 1 BOTTLE, SPRAY

Annotations

UNII (FDA Substance ID)
04JA59TNSJ
PHENYLEPHRINE HYDROCHLORIDE
RxCUI 8164
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "04JA59TNSJ",
    "rxcui": "8164",
    "inchikey": "OCYSGIYOVXAGKQ-FVGYRXGTSA-N",
    "display_name": "PHENYLEPHRINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "NASAL",
  "spl_meta": {
    "525467fb-510d-0b4b-e063-6294a90acd36": {
      "match": "brand_token",
      "title": "EXTRA STRENGTH TYLENOL COLD PLUS FLU MULTI-SYMPTOM NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE) LIQUID [KENVUE BRANDS LLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "70000-0132_411c9eb3-fe39-f3db-e063-6394a90a82df",
  "productndc": "70000-0132",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PHENYLEPHRINE HYDROCHLORIDE",
  "proprietary_name": "Extra Strength Sinus Relief Nasal Decongestant",
  "active_ingred_unit": "g/100mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Phenylephrine Hydrochloride",
  "start_marketing_date": "20170606",
  "active_numerator_strength": "1"
}

Related drugs

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