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United States · US · US:70677-1186_2b2c1d08-3320-d380-e063-6394a90a450c
Tussin
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerStrategic Sourcing Services
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170677118611 BOTTLE in 1 CARTON (70677-1186-1) / 118 mL in 1 BOTTLE
- ndc1170677118621 BOTTLE in 1 CARTON (70677-1186-2) / 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": {
"e1280355-da81-489f-9bd2-ffea9a68010c": {
"match": "brand_token",
"title": "TUSSIN COUGH AND CHEST CONGESTION DM ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [HARRIS TEETER, LLC]",
"spl_version": "3",
"published_date": "2026-04-30"
}
},
"productid": "70677-1186_2b2c1d08-3320-d380-e063-6394a90a450c",
"productndc": "70677-1186",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Tussin",
"active_ingred_unit": "mg/10mL",
"application_number": "part341",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20230809",
"active_numerator_strength": "200"
}Related drugs
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