nazal

Generic: naphazoline hydrochloride

Labeler: sato pharmaceutical co., ltd.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nazal
Generic Name naphazoline hydrochloride
Labeler sato pharmaceutical co., ltd.
Dosage Form LIQUID
Routes
NASAL
Active Ingredients

naphazoline hydrochloride 50 mg/100mL

Manufacturer
Sato Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 49873-057
Product ID 49873-057_0bde79a3-26b2-e0d2-e063-6294a90ac663
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 1990-06-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49873057
Hyphenated Format 49873-057

Supplemental Identifiers

RxCUI
1046602
UPC
0349873057019
UNII
MZ1131787D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nazal (source: ndc)
Generic Name naphazoline hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/100mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (49873-057-01) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

naphazoline hydrochloride (50 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "0bde79a3-26b2-e0d2-e063-6294a90ac663", "openfda": {"upc": ["0349873057019"], "unii": ["MZ1131787D"], "rxcui": ["1046602"], "spl_set_id": ["4d4043f8-5ed3-4027-beb6-687db1308202"], "manufacturer_name": ["Sato Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49873-057-01)  / 30 mL in 1 BOTTLE", "package_ndc": "49873-057-01", "marketing_start_date": "19900611"}], "brand_name": "Nazal", "product_id": "49873-057_0bde79a3-26b2-e0d2-e063-6294a90ac663", "dosage_form": "LIQUID", "product_ndc": "49873-057", "generic_name": "Naphazoline hydrochloride", "labeler_name": "Sato Pharmaceutical Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nazal", "active_ingredients": [{"name": "NAPHAZOLINE HYDROCHLORIDE", "strength": "50 mg/100mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19900611", "listing_expiration_date": "20261231"}