B&C Ointment

GUDID 00316477502566

Laser Pharmaceuticals, LLC

Skin semi-occlusive dressing, non-antimicrobial

• Primary Device ID: 00316477502566
• NIH Device Record Key: 962c7b36-da72-416c-9219-e642f79f8264
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: B&C Ointment
• Version Model Number: 1
• Company DUNS: 614417132
• Company Name: Laser Pharmaceuticals, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00316477502566 [Primary]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-15
• Device Publish Date: 2024-11-07

On-Brand Devices [B&C Ointment]

• 00316477502603: 1
• 00316477502566: 1