NDC 69473-007

Alumier MD Post Procedure Prescription

Titanium Dioxide, Zinc Oxide, Hydrocortisone Acetate

Alumier MD Post Procedure Prescription is a Topical Kit in the Human Otc Drug category. It is labeled and distributed by Alumier Labs. The primary component is .

• Product ID: 69473-007_8917ea86-a0d4-dd76-e053-2995a90acadd
• NDC: 69473-007
• Product Type: Human Otc Drug
• Proprietary Name: Alumier MD Post Procedure Prescription
• Generic Name: Titanium Dioxide, Zinc Oxide, Hydrocortisone Acetate
• Dosage Form: Kit
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-07-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Alumier Labs
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69473-007-01

1 KIT in 1 CARTON (69473-007-01) * 15 mL in 1 TUBE * 15 mL in 1 TUBE * 15 mL in 1 TUBE

• Marketing Start Date: 2019-07-01
• Marketing End Date: 2021-05-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69473-007-01 [69473000701]

Alumier MD Post Procedure Prescription KIT

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

Drug Details

OpenFDA Data

• SPL SET ID: 8917ea86-a0d3-dd76-e053-2995a90acadd
• Manufacturer:
  • Alumier Labs
• RxNorm Concept Unique ID - RxCUI:
  • 106258

NDC Crossover Matching brand name "Alumier MD Post Procedure Prescription" or generic name "Titanium Dioxide, Zinc Oxide, Hydrocortisone Acetate"

NDC	Brand Name	Generic Name
69473-007	Alumier MD Post Procedure Prescription	Titanium Dioxide, Zinc Oxide, Hydrocortisone Acetate
69473-013	Alumier MD Post Procedure Kit with Hydrocortisone	Titanium Dioxide, Zinc Oxide, Hydrocortisone Acetate