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United States · US · US:70000-0635_b06fcce1-b499-4f0d-a125-55d3ed7a3593
Leader Allergy Nasal
Orange BookUNIISPLATC D07AC13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 110, LLC. dba Leader
CountryUS (United States)
ATC codeD07AC13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170000063511 BOTTLE, SPRAY in 1 CARTON (70000-0635-1) / 60 SPRAY, METERED in 1 BOTTLE, SPRAY
- ndc1170000063521 BOTTLE, SPRAY in 1 CARTON (70000-0635-2) / 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": {
"12971fb2-2314-4443-bf70-b7eb5859b148": {
"match": "brand_token",
"title": "LEADER MUCUS RELIEF D (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, MULTILAYER, EXTENDED RELEASE [CARDINAL HEALTH 110, LLC. DBA LEADER]",
"spl_version": "3",
"published_date": "2026-06-01"
}
},
"productid": "70000-0635_b06fcce1-b499-4f0d-a125-55d3ed7a3593",
"productndc": "70000-0635",
"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": "Leader Allergy Nasal",
"active_ingred_unit": "ug/1",
"application_number": "NDA215712",
"marketing_category": "NDA",
"nonproprietary_name": "mometasone furoate",
"start_marketing_date": "20230922",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code D07AC13.
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