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    NDC 00023-6952-02 Refresh Digital 5; 10; 5 mg/mL; mg/mL; mg/mL Details

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

    Refresh Digital 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 00023-6952
    Product ID 0023-6952_2304c8bb-2ad8-4b78-a37d-0ba3d6ed88cf
    Associated GPIs 86209903202020
    GCN Sequence Number 069132
    GCN Sequence Number Description carboxymethyl/glycerin/poly80 DROPS 0.5-1-0.5% OPHTHALMIC
    HIC3 Q6T
    HIC3 Description ARTIFICIAL TEARS
    GCN 32087
    HICL Sequence Number 038941
    HICL Sequence Number Description CARBOXYMETHYLCELLULOSE SODIUM/GLYCERIN/POLYSORBATE 80
    Brand/Generic Brand
    Proprietary Name Refresh Digital
    Proprietary Name Suffix n/a
    Non-Proprietary Name Carboxymethylcellulose sodium, Glycerin, 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 00023-6952-02 (00023695202)

    NDC Package Code 0023-6952-02
    Billing NDC 00023695202
    Package 1 BOTTLE, DROPPER in 1 CARTON (0023-6952-02) / 2 mL in 1 BOTTLE, DROPPER
    Marketing Start Date 2020-08-01
    NDC Exclude Flag N
    Pricing Information N/A