NDC 10733-415

Salinocaine

Salicylic Acid And Benzocaine

Salinocaine is a Topical Ointment in the Human Prescription Drug category. It is labeled and distributed by Premier Dental Products. The primary component is Salicylic Acid; Benzocaine.

• Product ID: 10733-415_b4efca47-e929-4bb5-e053-2995a90aa56e
• NDC: 10733-415
• Product Type: Human Prescription Drug
• Proprietary Name: Salinocaine
• Generic Name: Salicylic Acid And Benzocaine
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 1938-06-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Premier Dental Products
• Substance Name: SALICYLIC ACID; BENZOCAINE
• Active Ingredient Strength: 550 mg/g; mg/g
• Pharm Classes: Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 10733-415-40

40 g in 1 JAR (10733-415-40)

• Marketing Start Date: 1998-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10733-415-40 [10733041540]

Salinocaine OINTMENT

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1938-06-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SALICYLIC ACID	550 mg/g

OpenFDA Data

• SPL SET ID: 49d9f83d-3055-f80e-e58a-b6fca192ac8d
• Manufacturer:
  • Medical Products Laboratories, Inc.
• UNII:
  • O414PZ4LPZ
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 1603382
  • 1603377

Pharmacological Class

• Standardized Chemical Allergen [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Allergens [CS]