NDC 71629-035

Willow Balm

Topical Pain Reliever

Willow Balm is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by I Woke Up Well Distributing Inc. The primary component is Menthol.

• Product ID: 71629-035_62d35ec4-83f1-a19a-e053-2a91aa0a863f
• NDC: 71629-035
• Product Type: Human Otc Drug
• Proprietary Name: Willow Balm
• Generic Name: Topical Pain Reliever
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-01-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: I Woke Up Well Distributing Inc
• Substance Name: MENTHOL
• Active Ingredient Strength: 0 g/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 71629-035-01

1 g in 1 TUBE (71629-035-01)

• Marketing Start Date: 2018-01-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71629-035-01 [71629003501]

Willow Balm CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-01-15

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL	.03 g/g

OpenFDA Data

• SPL SET ID: 62d35ec4-83f0-a19a-e053-2a91aa0a863f
• Manufacturer:
  • I Woke Up Well Distributing Inc
• UNII:
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 1442261

NDC Crossover Matching brand name "Willow Balm" or generic name "Topical Pain Reliever"

NDC	Brand Name	Generic Name
71629-035	Willow Balm	Topical Pain Reliever
73498-040	Natures Willow	Willow Balm
70743-0001	Uncle Buds	Topical Pain Reliever