saline
Generic: nasal
Labeler: publix super markets, incDrug Facts
Product Profile
Brand Name
saline
Generic Name
nasal
Labeler
publix super markets, inc
Dosage Form
SPRAY
Routes
Active Ingredients
sodium chloride 6.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
41415-477
Product ID
41415-477_4236dd11-5e52-416b-e063-6294a90a79b4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2021-01-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41415477
Hyphenated Format
41415-477
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 (41415-477-30) / 88 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": "4236dd11-5e52-416b-e063-6294a90a79b4", "openfda": {"upc": ["0041415478732"], "unii": ["451W47IQ8X"], "rxcui": ["707251"], "spl_set_id": ["19841567-9511-43d6-ba4e-d1e1bd3481a4"], "manufacturer_name": ["PUBLIX SUPER MARKETS, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41415-477-30) / 88 mL in 1 BOTTLE", "package_ndc": "41415-477-30", "marketing_start_date": "20210127"}], "brand_name": "Saline", "product_id": "41415-477_4236dd11-5e52-416b-e063-6294a90a79b4", "dosage_form": "SPRAY", "product_ndc": "41415-477", "generic_name": "Nasal", "labeler_name": "PUBLIX SUPER MARKETS, 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": "20210127", "listing_expiration_date": "20261231"}