refresh digital

Generic: carboxymethylcellulose sodium, glycerin, polysorbate 80

Labeler: allergan, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name refresh digital
Generic Name carboxymethylcellulose sodium, glycerin, polysorbate 80
Labeler allergan, inc.
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

carboxymethylcellulose sodium 5 mg/mL, glycerin 10 mg/mL, polysorbate 80 5 mg/mL

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0023-6952
Product ID 0023-6952_3da0fde5-6ea9-4a90-9470-d3f6e19a0630
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2027-12-31
Marketing Start 2020-08-01

Pharmacologic Class

Established (EPC)
non-standardized chemical allergen [epc]
Chemical Structure
allergens [cs] glycerol [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00236952
Hyphenated Format 0023-6952

Supplemental Identifiers

RxCUI
1241471
UNII
K679OBS311 PDC6A3C0OX 6OZP39ZG8H
NUI
N0000185370 N0000175629 N0000184306 N0000185001 M0000728 M0009417

Packaging Origin

Original Packager
true

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 digital (source: ndc)
Generic Name carboxymethylcellulose sodium, glycerin, polysorbate 80 (source: ndc)
Application Number M018 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (0023-6952-02) / 2 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (0023-6952-10) / 10 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (2)

0023-6952-02 1 BOTTLE, DROPPER in 1 CARTON (0023-6952-02) / 2 mL in 1 BOTTLE, DROPPER 0023-6952-10 1 BOTTLE, DROPPER in 1 CARTON (0023-6952-10) / 10 mL in 1 BOTTLE, DROPPER

Ingredients (3)

carboxymethylcellulose sodium (5 mg/mL) glycerin (10 mg/mL) polysorbate 80 (5 mg/mL)

Linked Drug Pages (1)

Refresh Digital ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "3da0fde5-6ea9-4a90-9470-d3f6e19a0630", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "unii": ["K679OBS311", "PDC6A3C0OX", "6OZP39ZG8H"], "rxcui": ["1241471"], "spl_set_id": ["b2bd34d4-fab9-4f4b-9be2-5d30b55f5b81"], "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": true, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-6952-02)  / 2 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-6952-02", "marketing_start_date": "20200801"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-6952-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-6952-10", "marketing_start_date": "20200801"}], "brand_name": "Refresh Digital", "product_id": "0023-6952_3da0fde5-6ea9-4a90-9470-d3f6e19a0630", "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": "0023-6952", "generic_name": "Carboxymethylcellulose sodium, Glycerin, Polysorbate 80", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Refresh Digital", "active_ingredients": [{"name": "CARBOXYMETHYLCELLULOSE SODIUM", "strength": "5 mg/mL"}, {"name": "GLYCERIN", "strength": "10 mg/mL"}, {"name": "POLYSORBATE 80", "strength": "5 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20271231"}