NDC 50157-114

SWIRLING LOLLIPOP

Antibacterial Hand Sanitizer Gel

SWIRLING LOLLIPOP is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Brands International Corp. The primary component is Alcohol.

• Product ID: 50157-114_2346dcb3-f1ba-6ba8-e054-00144ff8d46c
• NDC: 50157-114
• Product Type: Human Otc Drug
• Proprietary Name: SWIRLING LOLLIPOP
• Generic Name: Antibacterial Hand Sanitizer Gel
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2015-11-02
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: Brands International Corp
• Substance Name: ALCOHOL
• Active Ingredient Strength: 620 mL/1000mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50157-114-01

29 mL in 1 BOTTLE, PLASTIC (50157-114-01)

• Marketing Start Date: 2015-11-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50157-114-01 [50157011401]

SWIRLING LOLLIPOP GEL

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-11-02
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALCOHOL	620 mL/1000mL

OpenFDA Data

• SPL SET ID: 2346dcb3-f1b9-6ba8-e054-00144ff8d46c
• Manufacturer:
  • Brands International Corp
• UNII:
  • 3K9958V90M
• RxNorm Concept Unique ID - RxCUI:
  • 581660
• UPC Code:
  • 0672008802834

NDC Crossover Matching brand name "SWIRLING LOLLIPOP" or generic name "Antibacterial Hand Sanitizer Gel"

NDC	Brand Name	Generic Name
50157-114	SWIRLING LOLLIPOP	Antibacterial Hand Sanitizer Gel
50157-116	Bubble Gum	Antibacterial Hand Sanitizer Gel
50157-115	Japanese Cherry Blossom	Antibacterial Hand Sanitizer Gel
50157-300	Mint	Antibacterial Hand Sanitizer Gel