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United States · US · US:49873-057_0bde79a3-26b2-e0d2-e063-6294a90ac663
Nazal
UNIISPLATC R01AA08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSato Pharmaceutical Co., Ltd.
CountryUS (United States)
ATC codeR01AA08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1149873057011 BOTTLE in 1 CARTON (49873-057-01) / 30 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
MZ1131787D
NAPHAZOLINE HYDROCHLORIDE
RxCUI 82054
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "MZ1131787D",
"rxcui": "82054",
"inchikey": "DJDFFEBSKJCGHC-UHFFFAOYSA-N",
"display_name": "NAPHAZOLINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "NASAL",
"spl_meta": {
"4d4043f8-5ed3-4027-beb6-687db1308202": {
"match": "brand_token",
"title": "NAZAL (NAPHAZOLINE HYDROCHLORIDE) LIQUID [SATO PHARMACEUTICAL CO., LTD.]",
"spl_version": "7",
"published_date": "2023-12-07"
}
},
"productid": "49873-057_0bde79a3-26b2-e0d2-e063-6294a90ac663",
"productndc": "49873-057",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPHAZOLINE HYDROCHLORIDE",
"proprietary_name": "Nazal",
"active_ingred_unit": "mg/100mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Naphazoline hydrochloride",
"start_marketing_date": "19900611",
"active_numerator_strength": "50"
}Related drugs
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