NDC 69492-013

BIOACTIL

Pain Relieving

BIOACTIL is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Polimeros Y Servicios S.a.. The primary component is Menthol.

• Product ID: 69492-013_f0e928b1-0393-415d-a74f-4620538c219a
• NDC: 69492-013
• Product Type: Human Otc Drug
• Proprietary Name: BIOACTIL
• Generic Name: Pain Relieving
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-03-12
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: POLIMEROS Y SERVICIOS S.A.
• Substance Name: MENTHOL
• Active Ingredient Strength: 30 mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69492-013-07

1 TUBE in 1 BOX (69492-013-07) > 70 g in 1 TUBE

• Marketing Start Date: 2019-03-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69492-013-07 [69492001307]

BIOACTIL GEL

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-03-12

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL	30 mg/g

OpenFDA Data

• SPL SET ID: 744d7c69-6095-4d47-8f92-b685bf5ad00e
• Manufacturer:
  • POLIMEROS Y SERVICIOS S.A.
• UNII:
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 259150
• UPC Code:
  • 0851250006188

NDC Crossover Matching brand name "BIOACTIL" or generic name "Pain Relieving"

NDC	Brand Name	Generic Name
69492-013	BIOACTIL	Pain Relieving
68001-479	Pain Relieving	Pain Relieving