58161-156 NDC - DR.PHI ADVANCED HAND SANITIZER ()

Drug Information

Product NDC: 58161-156

Proprietary Name: Dr.Phi Advanced Hand sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: MAMIBA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2016

Package Information

No. Package Code Package Description Billing Unit
158161-156-0110 mL in 1 TUBE (58161-156-01)
258161-156-0250 mL in 1 BOTTLE, PLASTIC (58161-156-02)
358161-156-03315 mL in 1 BOTTLE, PLASTIC (58161-156-03)
458161-156-0415 mL in 1 POUCH (58161-156-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58161-156The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEDr.Phi Advanced Hand sanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMAMIBAName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC58161-156The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEDr.Phi Advanced Hand sanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMAMIBAName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023