sodium chloride hypertonicity

Generic: sodium chloride

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride hypertonicity
Generic Name sodium chloride
Labeler cvs pharmacy
Dosage Form OINTMENT
Routes
OPHTHALMIC
Active Ingredients

sodium chloride 50 mg/g

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 69842-285
Product ID 69842-285_48727bb0-e2bc-1eab-e063-6394a90a1144
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2027-12-31
Marketing Start 2020-05-01

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 69842285
Hyphenated Format 69842-285

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/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (69842-285-35) / 3.5 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

sodium chloride (50 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "48727bb0-e2bc-1eab-e063-6394a90a1144", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1298435"], "spl_set_id": ["d5cc6cd1-ddf8-4f5b-a021-204cdda0db94"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69842-285-35)  / 3.5 g in 1 TUBE", "package_ndc": "69842-285-35", "marketing_start_date": "20200501"}], "brand_name": "Sodium Chloride Hypertonicity", "product_id": "69842-285_48727bb0-e2bc-1eab-e063-6394a90a1144", "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": "69842-285", "generic_name": "sodium chloride", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Chloride Hypertonicity", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "50 mg/g"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200501", "listing_expiration_date": "20271231"}