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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 |
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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 |
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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 |