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NDC 58809-0221-30 DAYCLEAR ALLERGY RELIEF 25; 50 mg/1; mg/1 Details
DAYCLEAR ALLERGY RELIEF 25; 50 mg/1; mg/1
DAYCLEAR ALLERGY RELIEF is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by GM Pharmaceuticals, INC. The primary component is CHLOPHEDIANOL HYDROCHLORIDE; PYRILAMINE MALEATE.
Product Information
| NDC | 58809-0221 |
|---|---|
| Product ID | 58809-221_0b2780ac-ab93-dadd-e063-6394a90a83ca |
| Associated GPIs | 43995702450335 |
| GCN Sequence Number | 078909 |
| GCN Sequence Number Description | pyrilamine/chlophedianol TABLET 50 MG-25MG ORAL |
| HIC3 | B4E |
| HIC3 Description | NON-OPIOID ANTITUSSIVE-1ST GEN ANTIHISTAMINE COMB. |
| GCN | 45319 |
| HICL Sequence Number | 040404 |
| HICL Sequence Number Description | PYRILAMINE MALEATE/CHLOPHEDIANOL HCL |
| Brand/Generic | Brand |
| Proprietary Name | DAYCLEAR ALLERGY RELIEF |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Chlophedianol HCl, Pyrilamine Maleate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25; 50 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; PYRILAMINE MALEATE |
| Labeler Name | GM Pharmaceuticals, INC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M012 |
| Listing Certified Through | n/a |
Package
NDC 58809-0221-30 (58809022130)
| NDC Package Code | 58809-221-30 |
|---|---|
| Billing NDC | 58809022130 |
| Package | 30 TABLET in 1 BOTTLE (58809-221-30) |
| Marketing Start Date | 2018-08-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |