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United States · US · US:83324-217_45202ea0-a15c-7714-e063-6294a90a4bf5
QUALITY CHOICE
UNIISPLATC V06DC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
CountryUS (United States)
ATC codeV06DC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1183324217041 BOTTLE in 1 CARTON (83324-217-04) / 118 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
IY9XDZ35W2
DEXTROSE, UNSPECIFIED FORM
RxCUI 4850
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "IY9XDZ35W2",
"rxcui": "4850",
"inchikey": null,
"display_name": "DEXTROSE, UNSPECIFIED FORM",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d8fd8102-114f-415d-9083-f98a63f9d1b3": {
"match": "brand_token",
"title": "QUALITY CHOICE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE) LIQUID [CHAIN DRUG MARKETING ASSOCIATION, INC.]",
"spl_version": "4",
"published_date": "2026-06-01"
}
},
"productid": "83324-217_45202ea0-a15c-7714-e063-6294a90a4bf5",
"productndc": "83324-217",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID",
"proprietary_name": "QUALITY CHOICE",
"active_ingred_unit": "g/5mL; g/5mL; mg/5mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "dextrose(glucose),Levulose(fructose),Phosphoric acid",
"start_marketing_date": "20190416",
"active_numerator_strength": "1.87; 1.87; 21.5"
}Related drugs
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