allergy nasal

Orange BookUNIISPLATC D07AC13

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

Identification

ManufacturerWalgreen Company

CountryUS (United States)

ATC codeD07AC13

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0363206002
1 BOTTLE, SPRAY in 1 PACKAGE (0363-2060-02) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY

Annotations

UNII (FDA Substance ID)

MTW0WEG809

MOMETASONE FUROATE MONOHYDRATE

RxCUI 153374

Orange Book

N215712

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "MTW0WEG809",
    "rxcui": "153374",
    "inchikey": "AQCCVUHZMIMSIB-HRVPQZBTSA-N",
    "display_name": "MOMETASONE FUROATE MONOHYDRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "NASAL",
  "spl_meta": {
    "934c7b91-3cba-47f0-8efa-77216f3f15c4": {
      "match": "brand_token",
      "title": "ALLERGY RELIEF CHILDRENS (DIPHENHYDRAMINE HCL) TABLET, CHEWABLE [AMERISOURCE BERGEN]",
      "spl_version": "14",
      "published_date": "2026-06-01"
    }
  },
  "productid": "0363-2060_f7a19843-7bd4-4ab4-ad89-11bd951342db",
  "productndc": "0363-2060",
  "dosage_form": "SPRAY, METERED",
  "orange_book": {
    "appl_no": "215712",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "0.05MG/SPRAY",
        "product_no": "001",
        "approval_date": "Mar 17, 2022"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MOMETASONE FUROATE MONOHYDRATE",
  "proprietary_name": "allergy nasal",
  "active_ingred_unit": "ug/1",
  "application_number": "NDA215712",
  "marketing_category": "NDA",
  "nonproprietary_name": "mometasone furoate monohydrate",
  "start_marketing_date": "20230330",
  "active_numerator_strength": "50"
}

Related drugs

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