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NDC 00023-9537-05 Refresh RELIEVA PF 5; 10 mg/mL; mg/mL Details
Refresh RELIEVA PF 5; 10 mg/mL; mg/mL
Refresh RELIEVA 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.
Product Information
| NDC | 00023-9537 |
|---|---|
| Product ID | 0023-9537_9f04116b-954c-46e0-b755-d6273db959cd |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Refresh RELIEVA PF |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Carboxymethylcellulose sodium and Glycerin |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 5; 10 |
| Active Ingredient Units | mg/mL; mg/mL |
| Substance Name | CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN |
| 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 00023-9537-05 (00023953705)
| NDC Package Code | 0023-9537-05 |
|---|---|
| Billing NDC | 00023953705 |
| Package | 5 VIAL, SINGLE-USE in 1 CARTON (0023-9537-05) / .4 mL in 1 VIAL, SINGLE-USE |
| Marketing Start Date | 2020-09-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |