NDC 69329-011

Renuu NL

Allantoin, Petrolatum

Renuu NL is a Topical Patch in the Human Prescription Drug category. It is labeled and distributed by Patchwerx Labs. The primary component is Allantoin; Petrolatum.

• Product ID: 69329-011_172e582c-7e77-38ac-e054-00144ff88e88
• NDC: 69329-011
• Product Type: Human Prescription Drug
• Proprietary Name: Renuu NL
• Generic Name: Allantoin, Petrolatum
• Dosage Form: Patch
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-04-15
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Patchwerx Labs
• Substance Name: ALLANTOIN; PETROLATUM
• Active Ingredient Strength: 2 g/100g; g/100g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69329-011-15

15 PATCH in 1 BOX (69329-011-15) > 100 g in 1 PATCH (69329-011-01)

• Marketing Start Date: 2014-04-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69329-011-01 [69329001101]

Renuu NL PATCH

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-04-15

NDC 69329-011-15 [69329001115]

Renuu NL PATCH

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-04-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALLANTOIN	2 g/100g

OpenFDA Data

• SPL SET ID: 172e582c-7e76-38ac-e054-00144ff88e88
• Manufacturer:
  • Patchwerx Labs
• UNII:
  • 344S277G0Z
  • 4T6H12BN9U
• RxNorm Concept Unique ID - RxCUI:
  • 1651594