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NDC 00067-0106-06 Theraflu Severe Cold Relief Daytime Berry Burst 650; 20 mg/1; mg/1 Details
Theraflu Severe Cold Relief Daytime Berry Burst 650; 20 mg/1; mg/1
Theraflu Severe Cold Relief Daytime Berry Burst is a ORAL POWDER, FOR SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE.
Product Information
NDC | 00067-0106 |
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Product ID | 0067-0106_0bbbc931-acd0-6e0c-e063-6294a90acd3e |
Associated GPIs | 46300048003000 |
GCN Sequence Number | 064401 |
GCN Sequence Number Description | wheat dextrin/aspartame POWD PACK 3 G/6 G ORAL |
HIC3 | D6S |
HIC3 Description | LAXATIVES AND CATHARTICS |
GCN | 14237 |
HICL Sequence Number | 035855 |
HICL Sequence Number Description | WHEAT DEXTRIN/ASPARTAME |
Brand/Generic | Brand |
Proprietary Name | Theraflu Severe Cold Relief Daytime Berry Burst |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HBr |
Product Type | HUMAN OTC DRUG |
Dosage Form | POWDER, FOR SOLUTION |
Route | ORAL |
Active Ingredient Strength | 650; 20 |
Active Ingredient Units | mg/1; mg/1 |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE |
Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
Pharmaceutical Class | Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH DRUG |
Application Number | M012 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00067-0106-06 (00067010606)
NDC Package Code | 0067-0106-06 |
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Billing NDC | 00067010606 |
Package | 6 PACKET in 1 CARTON (0067-0106-06) / 1 POWDER, FOR SOLUTION in 1 PACKET |
Marketing Start Date | 2023-12-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |