NDC 0067-6094

Theraflu PowerPods Daytime Severe Cold

Acetaminophen, Dextromethorphan, Phenylephrine

Theraflu PowerPods Daytime Severe Cold 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; Phenylephrine Hydrochloride.

• Product ID: 0067-6094_76f40bbc-261d-4a92-af8f-a7930bf3f167
• NDC: 0067-6094
• Product Type: Human Otc Drug
• Proprietary Name: Theraflu PowerPods Daytime Severe Cold
• Generic Name: Acetaminophen, Dextromethorphan, Phenylephrine
• Dosage Form: Powder, For Solution
• Route of Administration: ORAL
• Marketing Start Date: 2018-07-28
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Substance Name: ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
• Active Ingredient Strength: 650 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0067-6094-01

8 POUCH in 1 CARTON (0067-6094-01) > 1 POWDER, FOR SOLUTION in 1 POUCH (0067-6094-02)

• Marketing Start Date: 2018-07-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0067-6094-01 [00067609401]

Theraflu PowerPods Daytime Severe Cold POWDER, FOR SOLUTION

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-28

NDC 0067-6094-02 [00067609402]

Theraflu PowerPods Daytime Severe Cold POWDER, FOR SOLUTION

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-28

NDC 0067-6094-03 [00067609403]

Theraflu PowerPods Daytime Severe Cold POWDER, FOR SOLUTION

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-01-20

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	650 mg/1

OpenFDA Data

• SPL SET ID: e655c33c-c319-41d9-ae55-cf747242cd10
• Manufacturer:
  • GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• UNII:
  • 362O9ITL9D
  • 04JA59TNSJ
  • 9D2RTI9KYH
• RxNorm Concept Unique ID - RxCUI:
  • 1659967

NDC Crossover Matching brand name "Theraflu PowerPods Daytime Severe Cold" or generic name "Acetaminophen, Dextromethorphan, Phenylephrine"

NDC	Brand Name	Generic Name
59779-776	CVS Daytime Severe Cough and Cold	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
67510-0544	Day Time Cold/Flu Relief	Acetaminophen, Dextromethorphan, Phenylephrine
59970-077	Day Time Gelcap	Acetaminophen, Dextromethorphan, Phenylephrine
67510-0523	Day Time Gelcap	Acetaminophen, Dextromethorphan, Phenylephrine
69517-102	DayTime Cold and Flu Relief	Acetaminophen, Dextromethorphan, Phenylephrine
63561-1129	end-a-flu	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
63561-0129	FLU-MED	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
63868-290	Severe Cold and Cough Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
67091-322	Severe Cold and Cough Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
0067-6094	Theraflu	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
0067-7917	Theraflu	ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
52904-896	Theraflu Daytime Severe Cold and Cough	acetaminophen, dextromethorphan, phenylephrine