NDC 54473-185

CounterAct Day

Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine

CounterAct Day is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Melaleuca, Inc.. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.

• Product ID: 54473-185_65e42ef2-d090-6174-e053-2991aa0a9830
• NDC: 54473-185
• Product Type: Human Otc Drug
• Proprietary Name: CounterAct Day
• Generic Name: Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2011-10-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Melaleuca, Inc.
• Substance Name: ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
• Active Ingredient Strength: 325 mg/1; mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 54473-185-36

3 BLISTER PACK in 1 BOX (54473-185-36) > 12 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2018-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54473-185-36 [54473018536]

CounterAct Day TABLET, FILM COATED

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-01-01
• Marketing End Date: 2019-12-31

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 mg/1

OpenFDA Data

• SPL SET ID: 07ee5376-e907-4183-b49a-67f5e894836c
• Manufacturer:
  • Melaleuca, Inc.
• UNII:
  • 362O9ITL9D
  • 04JA59TNSJ
  • 9D2RTI9KYH
  • 495W7451VQ
• RxNorm Concept Unique ID - RxCUI:
  • 1110988