sodium chloride hypertonicity

Generic: sodium chloride

Labeler: yyba corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride hypertonicity
Generic Name sodium chloride
Labeler yyba corp
Dosage Form OINTMENT
Routes
OPHTHALMIC
Active Ingredients

sodium chloride 50 mg/mL

Manufacturer
YYBA CORP

Identifiers & Regulatory

Product NDC 73581-708
Product ID 73581-708_214c5b0a-d501-3c0f-e063-6294a90a4509
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2026-12-31
Marketing Start 2024-08-12

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73581708
Hyphenated Format 73581-708

Supplemental Identifiers

RxCUI
1298435
UNII
451W47IQ8X

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 sodium chloride hypertonicity (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number M018 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (73581-708-35) / 3.5 mL in 1 TUBE
source: ndc

Packages (1)

73581-708-35 1 TUBE in 1 CARTON (73581-708-35) / 3.5 mL in 1 TUBE

Ingredients (1)

sodium chloride (50 mg/mL)

Linked Drug Pages (1)

SODIUM CHLORIDE HYPERTONICITY ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "214c5b0a-d501-3c0f-e063-6294a90a4509", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1298435"], "spl_set_id": ["439653b9-99b8-4799-8d67-4a2ada9c6783"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (73581-708-35)  / 3.5 mL in 1 TUBE", "package_ndc": "73581-708-35", "marketing_start_date": "20240812"}], "brand_name": "SODIUM CHLORIDE HYPERTONICITY", "product_id": "73581-708_214c5b0a-d501-3c0f-e063-6294a90a4509", "dosage_form": "OINTMENT", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "73581-708", "generic_name": "sodium chloride", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SODIUM CHLORIDE HYPERTONICITY", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "50 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240812", "listing_expiration_date": "20261231"}