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    NDC 00023-6954-05 Refresh Digital PF 5; 10; 5 mg/mL; mg/mL; mg/mL Details

    Refresh Digital PF 5; 10; 5 mg/mL; mg/mL; mg/mL

    Refresh Digital PF is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Allergan, Inc.. The primary component is CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80.

    Product Information

    NDC 00023-6954
    Product ID 0023-6954_0702ebf0-06fb-44a1-ba8b-21c00c4a288d
    Associated GPIs 86209903202022
    GCN Sequence Number 070905
    GCN Sequence Number Description carboxymethyl/gly/poly80/PF DROPERETTE 0.5-1-0.5% OPHTHALMIC
    HIC3 Q6T
    HIC3 Description ARTIFICIAL TEARS
    GCN 34571
    HICL Sequence Number 040248
    HICL Sequence Number Description CARBOXYMETHYLCELLULOSE SODIUM/GLYCERIN/POLYSORBATE 80/PF
    Brand/Generic Brand
    Proprietary Name Refresh Digital PF
    Proprietary Name Suffix n/a
    Non-Proprietary Name Carboxymethylcellulose sodium, Glycerin and Polysorbate 80
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION/ DROPS
    Route OPHTHALMIC
    Active Ingredient Strength 5; 10; 5
    Active Ingredient Units mg/mL; mg/mL; mg/mL
    Substance Name CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
    Labeler Name Allergan, Inc.
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M018
    Listing Certified Through 2024-12-31

    Package

    NDC 00023-6954-05 (00023695405)

    NDC Package Code 0023-6954-05
    Billing NDC 00023695405
    Package 1 VIAL, PLASTIC in 1 CARTON (0023-6954-05) / .4 mL in 1 VIAL, PLASTIC
    Marketing Start Date 2020-08-01
    NDC Exclude Flag N
    Pricing Information N/A