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United States · US · US:16030-401_495c0c2e-380d-b1c0-e063-6394a90aa33b
AURO-CMC
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurolab
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11160304011010 mL in 1 BOTTLE, DROPPER (16030-401-10)
Annotations
UNII (FDA Substance ID)
K679OBS311
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
RxCUI 491498
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "K679OBS311",
"rxcui": "491498",
"inchikey": null,
"display_name": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"e90b397f-fe64-8674-e053-2995a90a223f": {
"match": "brand_token",
"title": "AURO-CMC (CARBOXYMETHYLCELLULOSE EYE DROPS 0.5%) FOR SOLUTION [AUROLAB]",
"spl_version": "7",
"published_date": "2026-01-28"
}
},
"productid": "16030-401_495c0c2e-380d-b1c0-e063-6394a90aa33b",
"productndc": "16030-401",
"dosage_form": "FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
"proprietary_name": "AURO-CMC",
"active_ingred_unit": "mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Carboxymethylcellulose Eye Drops 0.5%",
"start_marketing_date": "20220920",
"active_numerator_strength": "5"
}Access this data programmatically
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