🇺🇸
United States · US · US:70000-0696_d7fae410-9c1c-4231-9fde-2c51ad3d7e95
Leader Adult Tussin Mucus and Chest Congestion 541
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCARDINAL HEALTH 110, LLC. DBA LEADER
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170000069611 BOTTLE in 1 CARTON (70000-0696-1) / 118 mL in 1 BOTTLE
- ndc1170000069621 BOTTLE in 1 CARTON (70000-0696-2) / 237 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "495W7451VQ",
"rxcui": "5032",
"inchikey": "HSRJKNPTNIJEKV-UHFFFAOYSA-N",
"display_name": "GUAIFENESIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"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": "70000-0696_d7fae410-9c1c-4231-9fde-2c51ad3d7e95",
"productndc": "70000-0696",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Leader Adult Tussin Mucus and Chest Congestion 541",
"active_ingred_unit": "mg/10mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20240920",
"active_numerator_strength": "200"
}Related drugs
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