NDC 24438-001

Phoenix Balm

Pain Relief Rub

Phoenix Balm is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Amazonian Naturals, Inc.. The primary component is Camphor (natural); Menthol; Methyl Salicylate.

• Product ID: 24438-001_fab49a9f-9c0f-4a00-81cf-c9bbd5ef0826
• NDC: 24438-001
• Product Type: Human Otc Drug
• Proprietary Name: Phoenix Balm
• Generic Name: Pain Relief Rub
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-12-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part348
• Labeler Name: Amazonian Naturals, Inc.
• Substance Name: CAMPHOR (NATURAL); MENTHOL; METHYL SALICYLATE
• Active Ingredient Strength: 50 mg/g; mg/g; mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 24438-001-02

1 CONTAINER in 1 BOX (24438-001-02) > 19 g in 1 CONTAINER (24438-001-01)

• Marketing Start Date: 2011-12-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 24438-001-01 [24438000101]

Phoenix Balm OINTMENT

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-01

NDC 24438-001-02 [24438000102]

Phoenix Balm OINTMENT

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
CAMPHOR (NATURAL)	50 mg/g

OpenFDA Data

• SPL SET ID: 1ee482e2-155b-4f82-ab90-0457911806a8
• Manufacturer:
  • Amazonian Naturals, Inc.
• UNII:
  • L7T10EIP3A
  • N20HL7Q941
  • LAV5U5022Y
• RxNorm Concept Unique ID - RxCUI:
  • 1232398