NDC 41250-701

Oral Analgesic Maximum Strength

Oral Pain Reliever

Oral Analgesic Maximum Strength is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Meijer Distribution, Inc.. The primary component is Benzocaine.

• Product ID: 41250-701_51e14b50-af28-4132-873a-37e904549c1d
• NDC: 41250-701
• Product Type: Human Otc Drug
• Proprietary Name: Oral Analgesic Maximum Strength
• Generic Name: Oral Pain Reliever
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-05-13
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Meijer Distribution, Inc.
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 200 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 41250-701-25

1 TUBE in 1 CARTON (41250-701-25) > 7.1 g in 1 TUBE

• Marketing Start Date: 2010-05-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 41250-701-25 [41250070125]

Oral Analgesic Maximum Strength GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-13
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	200 mg/g

OpenFDA Data

• SPL SET ID: 5372eea1-afd5-4bde-8d76-f6b0aaffc199
• Manufacturer:
  • Meijer Distribution, Inc.
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 238910
• UPC Code:
  • 0000000000000

NDC Crossover Matching brand name "Oral Analgesic Maximum Strength" or generic name "Oral Pain Reliever"

NDC	Brand Name	Generic Name
41250-703	Oral Analgesic Maximum Strength	Oral Analgesic Maximum Strength
41250-706	Oral Analgesic Maximum Strength	Oral Analgesic Maximum Strength
51852-101	Oral Analgesic Maximum Strength	Oral Analgesic Maximum Strength
41250-701	Oral Analgesic	Oral Pain Reliever
53943-996	Oral Pain Relief	Oral Pain Reliever
67510-0058	Oral Pain Relief	Oral Pain Reliever