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NDC 41163-0334-12 Headache Relief 250; 250; 65 mg/1; mg/1; mg/1 Details
Headache Relief 250; 250; 65 mg/1; mg/1; mg/1
Headache Relief is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by United Natural Foods, Inc. dba UNFI. The primary component is ACETAMINOPHEN; ASPIRIN; CAFFEINE.
Product Information
NDC | 41163-0334 |
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Product ID | 41163-334_b4f3ad08-e699-4ef0-b0dd-11b111d22f4b |
Associated GPIs | |
GCN Sequence Number | 040186 |
GCN Sequence Number Description | aspirin/acetaminophen/caffeine TABLET 250-250-65 ORAL |
HIC3 | H3D |
HIC3 Description | ANALGESIC/ANTIPYRETICS, SALICYLATES |
GCN | 10414 |
HICL Sequence Number | 001807 |
HICL Sequence Number Description | ASPIRIN/ACETAMINOPHEN/CAFFEINE |
Brand/Generic | Generic |
Proprietary Name | Headache Relief |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | acetaminophen, aspirin, caffeine |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 250; 250; 65 |
Active Ingredient Units | mg/1; mg/1; mg/1 |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Labeler Name | United Natural Foods, Inc. dba UNFI |
Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [E |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH DRUG |
Application Number | M013 |
Listing Certified Through | 2024-12-31 |
Package
NDC 41163-0334-12 (41163033412)
NDC Package Code | 41163-334-12 |
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Billing NDC | 41163033412 |
Package | 1 BOTTLE, PLASTIC in 1 CARTON (41163-334-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
Marketing Start Date | 2017-11-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |