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NDC 00280-0020-01 Alka-Seltzer Plus Severe Cold PowerFast Fizz 325; 2; 7 mg/1; mg/1; mg/1 Details
Alka-Seltzer Plus Severe Cold PowerFast Fizz 325; 2; 7 mg/1; mg/1; mg/1
Alka-Seltzer Plus Severe Cold PowerFast Fizz is a ORAL TABLET, EFFERVESCENT in the HUMAN OTC DRUG category. It is labeled and distributed by Bayer HealthCare LLC.. The primary component is ASPIRIN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE BITARTRATE.
Product Information
NDC | 00280-0020 |
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Product ID | 0280-0020_030bc78e-6d7d-06cb-e063-6394a90afa70 |
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 | Alka-Seltzer Plus Severe Cold PowerFast Fizz |
Proprietary Name Suffix | Orange Zest |
Non-Proprietary Name | aspirin, chlorpheniramine maleate, phenylephrine bitartrate |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, EFFERVESCENT |
Route | ORAL |
Active Ingredient Strength | 325; 2; 7 |
Active Ingredient Units | mg/1; mg/1; mg/1 |
Substance Name | ASPIRIN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE BITARTRATE |
Labeler Name | Bayer HealthCare LLC. |
Pharmaceutical Class | Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor An |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00280-0020-01 (00280002001)
NDC Package Code | 0280-0020-01 |
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Billing NDC | 00280002001 |
Package | 10 POUCH in 1 CARTON (0280-0020-01) / 2 TABLET, EFFERVESCENT in 1 POUCH |
Marketing Start Date | 2020-07-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |