NDC 10237-703

Orajel Maximum Strength

Benzocaine

Orajel Maximum Strength is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Church & Dwight Co., Inc.. The primary component is Benzocaine.

• Product ID: 10237-703_52266132-3a1c-471d-96a3-a8e1c0c4bdaf
• NDC: 10237-703
• Product Type: Human Otc Drug
• Proprietary Name: Orajel Maximum Strength
• Generic Name: Benzocaine
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-04-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Church & Dwight Co., Inc.
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 0 mL/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 10237-703-45

1 BOTTLE, GLASS in 1 CARTON (10237-703-45) > 13.3 mL in 1 BOTTLE, GLASS

• Marketing Start Date: 2010-04-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10237-703-45 [10237070345]

Orajel Maximum Strength LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-04-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	.2 mL/mL

OpenFDA Data

• SPL SET ID: 8ce643ea-5f8d-4ae9-b1ff-6b04196f4b4f
• Manufacturer:
  • Church & Dwight Co., Inc.
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 308657
  • 1045335

NDC Crossover Matching brand name "Orajel Maximum Strength" or generic name "Benzocaine"

NDC	Brand Name	Generic Name
10237-703	Orajel Maximum Strength	Orajel Maximum Strength
0283-0220	HurriCaine	Benzocaine
0283-0293	HurriCaine	Benzocaine
0283-0520	HurriCaine	Benzocaine
0283-0569	HurriCaine	Benzocaine
0283-0679	HurriCaine	Benzocaine
0283-0871	HurriCaine	BENZOCAINE
0283-0886	HurriCaine	Benzocaine
0283-0914	HurriCaine	Benzocaine
0283-0920	HurriCaine	Benzocaine
0283-0998	HurriCaine	Benzocaine
0283-1016	HurriCaine	BENZOCAINE