NDC 58161-155

Dr.Phi Instant Hand Sanitizer

Dr.phi Instant Hand Sanitizer

Dr.Phi Instant Hand Sanitizer is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Mamiba. The primary component is Alcohol.

• Product ID: 58161-155_5087f840-3789-4245-83cf-62aac3c7bf6d
• NDC: 58161-155
• Product Type: Human Otc Drug
• Proprietary Name: Dr.Phi Instant Hand Sanitizer
• Generic Name: Dr.phi Instant Hand Sanitizer
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-09-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: MAMIBA
• Substance Name: ALCOHOL
• Active Ingredient Strength: 1 mL/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 58161-155-02

36 TUBE in 1 PACKAGE (58161-155-02) > 10 mL in 1 TUBE (58161-155-01)

• Marketing Start Date: 2014-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58161-155-01 [58161015501]

Dr.Phi Instant Hand Sanitizer GEL

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-09-01

NDC 58161-155-02 [58161015502]

Dr.Phi Instant Hand Sanitizer GEL

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-09-01
• Inactivation Date: 2019-11-27

NDC 58161-155-03 [58161015503]

Dr.Phi Instant Hand Sanitizer GEL

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-09-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
ALCOHOL	.7 mL/mL

OpenFDA Data

• SPL SET ID: 6e03d260-7da7-45be-b951-7fccc219edf6
• Manufacturer:
  • MAMIBA
• UNII:
  • 3K9958V90M
• RxNorm Concept Unique ID - RxCUI:
  • 581662