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United States · US · US:69230-332_62155505-522d-4269-8d03-599c6d2c902c
Adult Tussin
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCamber Consumer Care
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169230332231 BOTTLE in 1 CARTON (69230-332-23) / 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": {
"47b713bd-4c1e-f44a-e063-6294a90a63d3": {
"match": "brand_token",
"title": "ADULT COUGH SUPPRESSANT DEXTROMETHORPHAN HBR (DEXTROMETHORPHAN HYDROBROMIDE) CAPSULE, LIQUID FILLED [RUGBY LABORATORIES]",
"spl_version": "2",
"published_date": "2026-05-14"
}
},
"productid": "69230-332_62155505-522d-4269-8d03-599c6d2c902c",
"productndc": "69230-332",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Adult Tussin",
"active_ingred_unit": "mg/10mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "GUAIFENESIN",
"start_marketing_date": "20250519",
"active_numerator_strength": "200"
}Related drugs
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