saline
Generic: nasal
Labeler: raritan pharmaceuiticals incDrug Facts
Product Profile
Brand Name
saline
Generic Name
nasal
Labeler
raritan pharmaceuiticals inc
Dosage Form
SPRAY
Routes
Active Ingredients
sodium chloride 6.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68163-704
Product ID
68163-704_3fee4ab2-7a54-e8b8-e063-6394a90a0fa0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2020-09-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68163704
Hyphenated Format
68163-704
Supplemental Identifiers
RxCUI
UPC
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
saline (source: ndc)
Generic Name
nasal (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6.5 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (68163-704-15) / 44 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "3fee4ab2-7a54-e8b8-e063-6394a90a0fa0", "openfda": {"upc": ["0368163704150"], "unii": ["451W47IQ8X"], "rxcui": ["707251"], "spl_set_id": ["4b178e4e-a10f-4b75-8140-1f7548e203ad"], "manufacturer_name": ["Raritan Pharmaceuiticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68163-704-15) / 44 mL in 1 BOTTLE", "package_ndc": "68163-704-15", "marketing_start_date": "20200930"}], "brand_name": "Saline", "product_id": "68163-704_3fee4ab2-7a54-e8b8-e063-6394a90a0fa0", "dosage_form": "SPRAY", "product_ndc": "68163-704", "generic_name": "Nasal", "labeler_name": "Raritan Pharmaceuiticals Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Saline", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "6.5 mg/mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}