family care saline
Generic: sodium chloride
Labeler: united exchange corp.Drug Facts
Product Profile
Brand Name
family care saline
Generic Name
sodium chloride
Labeler
united exchange corp.
Dosage Form
SPRAY
Routes
Active Ingredients
sodium chloride 6.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65923-493
Product ID
65923-493_427c79ab-bf9e-cc4c-e063-6294a90a8485
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2023-09-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65923493
Hyphenated Format
65923-493
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
family care saline (source: ndc)
Generic Name
sodium chloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6.5 mg/mL
Packaging
- 44 mL in 1 BOTTLE, SPRAY (65923-493-44)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "427c79ab-bf9e-cc4c-e063-6294a90a8485", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["707251"], "spl_set_id": ["06737393-d4ae-3e7b-e063-6394a90ac19f"], "manufacturer_name": ["United Exchange Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "44 mL in 1 BOTTLE, SPRAY (65923-493-44)", "package_ndc": "65923-493-44", "marketing_start_date": "20230928"}], "brand_name": "Family Care Saline", "product_id": "65923-493_427c79ab-bf9e-cc4c-e063-6294a90a8485", "dosage_form": "SPRAY", "product_ndc": "65923-493", "generic_name": "Sodium Chloride", "labeler_name": "United Exchange Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Family Care Saline", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "6.5 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230928", "listing_expiration_date": "20261231"}