NDC 51532-0107

Chloresin

Acetaminophen, Dextromethorphan, Guaifenesin, Phenylephrine

Chloresin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Affasco Inc.. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.

• Product ID: 51532-0107_16381a80-13b7-4929-a4cb-f1a7148f45cd
• NDC: 51532-0107
• Product Type: Human Otc Drug
• Proprietary Name: Chloresin
• Generic Name: Acetaminophen, Dextromethorphan, Guaifenesin, Phenylephrine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-10-25
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Affasco Inc.
• Substance Name: ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
• Active Ingredient Strength: 325 1/1; 1/1; 1/1; 1/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51532-0107-2

2 TABLET in 1 PACKET (51532-0107-2)

• Marketing Start Date: 2016-10-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51532-0107-2 [51532010702]

Chloresin TABLET

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-10-25

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 1/1

OpenFDA Data

• SPL SET ID: 77a5f0d0-18cf-4618-85b7-90c86a1f2e23
• Manufacturer:
  • Affasco Inc.
• UNII:
  • 362O9ITL9D
  • 04JA59TNSJ
  • 9D2RTI9KYH
  • 495W7451VQ
• RxNorm Concept Unique ID - RxCUI:
  • 1367204