normal salt
Generic: sodium chloride
Labeler: twin med llcDrug Facts
Product Profile
Brand Name
normal salt
Generic Name
sodium chloride
Labeler
twin med llc
Dosage Form
TABLET
Routes
Active Ingredients
sodium chloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
55681-305
Product ID
55681-305_3906d64f-c399-ab67-e063-6294a90ad159
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Marketing Start
2021-01-03
Marketing End
2027-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55681305
Hyphenated Format
55681-305
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
normal salt (source: ndc)
Generic Name
sodium chloride (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 200 TABLET in 1 BOTTLE (55681-305-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3906d64f-c399-ab67-e063-6294a90ad159", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["313009"], "spl_set_id": ["dc82ff0f-8600-373a-e053-2995a90a7505"], "manufacturer_name": ["Twin Med LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (55681-305-03)", "package_ndc": "55681-305-03", "marketing_end_date": "20271231", "marketing_start_date": "20220401"}], "brand_name": "Normal Salt", "product_id": "55681-305_3906d64f-c399-ab67-e063-6294a90ad159", "dosage_form": "TABLET", "product_ndc": "55681-305", "generic_name": "Sodium Chloride", "labeler_name": "Twin Med LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Normal Salt", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "1 g/1"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20271231", "marketing_start_date": "20210103"}