NDC 63922-605

KGS ALLERGY SOOTHING

Acetaminophen Chlorpheniramine Maleate

KGS ALLERGY SOOTHING is a Oral Capsule, Delayed Release Pellets in the Human Otc Drug category. It is labeled and distributed by Kingsway. The primary component is Acetaminophen; Chlorpheniramine Maleate.

• Product ID: 63922-605_dc8d6626-3092-43cb-94c8-a2a02d4b321b
• NDC: 63922-605
• Product Type: Human Otc Drug
• Proprietary Name: KGS ALLERGY SOOTHING
• Generic Name: Acetaminophen Chlorpheniramine Maleate
• Dosage Form: Capsule, Delayed Release Pellets
• Route of Administration: ORAL
• Marketing Start Date: 2014-01-30
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Kingsway
• Substance Name: ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE
• Active Ingredient Strength: 250 mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63922-605-01

1 BLISTER PACK in 1 BOX (63922-605-01) > 12 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (63922-605-12)

• Marketing Start Date: 2014-01-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63922-605-01 [63922060501]

KGS ALLERGY SOOTHING CAPSULE, DELAYED RELEASE PELLETS

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-30
• Inactivation Date: 2019-11-27

NDC 63922-605-12 [63922060512]

KGS ALLERGY SOOTHING CAPSULE, DELAYED RELEASE PELLETS

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-30

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	250 mg/1

OpenFDA Data

• SPL SET ID: 0a205049-811f-4f66-ac29-cb2a7b4efbf0
• Manufacturer:
  • Kingsway
• UNII:
  • V1Q0O9OJ9Z
  • 362O9ITL9D
• UPC Code:
  • 0363922216448