refresh relieva pf xtra
Generic: carboxymethylcellulose sodium and glycerin
Labeler: allergan, inc.Drug Facts
Product Profile
Brand Name
refresh relieva pf xtra
Generic Name
carboxymethylcellulose sodium and glycerin
Labeler
allergan, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
carboxymethylcellulose sodium 5 mg/mL, glycerin 9 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0023-3782
Product ID
0023-3782_2647691e-a3b2-44e1-bcdc-a1a256a37912
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M018
Listing Expiration
2026-12-31
Marketing Start
2024-03-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00233782
Hyphenated Format
0023-3782
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
refresh relieva pf xtra (source: ndc)
Generic Name
carboxymethylcellulose sodium and glycerin (source: ndc)
Application Number
M018 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
- 9 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-10) / 10 mL in 1 BOTTLE, DROPPER
- 2 BOTTLE, DROPPER in 1 CARTON (0023-3782-20) / 10 mL in 1 BOTTLE, DROPPER
- 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-35) / 10 mL in 1 BOTTLE, DROPPER
- 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-50) / 3.5 mL in 1 BOTTLE, DROPPER
Packages (4)
0023-3782-10
1 BOTTLE, DROPPER in 1 CARTON (0023-3782-10) / 10 mL in 1 BOTTLE, DROPPER
0023-3782-20
2 BOTTLE, DROPPER in 1 CARTON (0023-3782-20) / 10 mL in 1 BOTTLE, DROPPER
0023-3782-35
1 BOTTLE, DROPPER in 1 CARTON (0023-3782-35) / 10 mL in 1 BOTTLE, DROPPER
0023-3782-50
1 BOTTLE, DROPPER in 1 CARTON (0023-3782-50) / 3.5 mL in 1 BOTTLE, DROPPER
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2647691e-a3b2-44e1-bcdc-a1a256a37912", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "upc": ["0300233782101"], "unii": ["K679OBS311", "PDC6A3C0OX"], "rxcui": ["1100650"], "spl_set_id": ["b51b8a75-8faa-430f-8f7e-ee58d3d13f2e"], "pharm_class_cs": ["Allergens [CS]", "Glycerol [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3782-10) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3782-10", "marketing_start_date": "20240301"}, {"sample": false, "description": "2 BOTTLE, DROPPER in 1 CARTON (0023-3782-20) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3782-20", "marketing_start_date": "20251015"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3782-35) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3782-35", "marketing_start_date": "20240301"}, {"sample": true, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3782-50) / 3.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3782-50", "marketing_start_date": "20240301"}], "brand_name": "Refresh Relieva PF Xtra", "product_id": "0023-3782_2647691e-a3b2-44e1-bcdc-a1a256a37912", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Glycerol [CS]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Chemical Allergen [EPC]"], "product_ndc": "0023-3782", "generic_name": "Carboxymethylcellulose Sodium and Glycerin", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Refresh Relieva PF Xtra", "active_ingredients": [{"name": "CARBOXYMETHYLCELLULOSE SODIUM", "strength": "5 mg/mL"}, {"name": "GLYCERIN", "strength": "9 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}