NDC 20276-561

Lucky Oral Pain Relief

Benzocaine Benzalkonium Chloride

Lucky Oral Pain Relief is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Delta Brands Inc. The primary component is Benzocaine; Benzalkonium Chloride.

• Product ID: 20276-561_6d3a3406-d5f3-4d7d-8898-79d9a4682776
• NDC: 20276-561
• Product Type: Human Otc Drug
• Proprietary Name: Lucky Oral Pain Relief
• Generic Name: Benzocaine Benzalkonium Chloride
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-06-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Delta Brands Inc
• Substance Name: BENZOCAINE; BENZALKONIUM CHLORIDE
• Active Ingredient Strength: 20 g/100g; g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 20276-561-14

14 g in 1 TUBE (20276-561-14)

• Marketing Start Date: 2014-06-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 20276-561-14 [20276056114]

Lucky Oral Pain Relief GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-06-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	20 g/100g

OpenFDA Data

• SPL SET ID: 5dbfa3ae-2994-45d5-b799-a2638d87d9e8
• Manufacturer:
  • Delta Brands Inc
• UNII:
  • F5UM2KM3W7
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 1595155

NDC Crossover Matching brand name "Lucky Oral Pain Relief" or generic name "Benzocaine Benzalkonium Chloride"

NDC	Brand Name	Generic Name
33992-2013	Assured	Benzocaine Benzalkonium chloride
27293-020	Budpack	Benzocaine Benzalkonium chloride
20276-561	Lucky	Benzocaine Benzalkonium Chloride
47046-169	Lucky	Benzocaine Benzalkonium Chloride
69020-209	MakeSense	Benzocaine Benzalkonium chloride
76038-091	MEDITOWEL	BENZOCAINE BENZALKONIUM CHLORIDE