67777-317 NDC - SANNYTIZE HAND SANITIZER ()

Drug Information

Product NDC: 67777-317

Proprietary Name: SannyTize Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dynarex Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/25/2017

Package Information

No. Package Code Package Description Billing Unit
167777-317-0129.5 mL in 1 BOTTLE (67777-317-01)
267777-317-0259 mL in 1 BOTTLE (67777-317-02)
367777-317-03118 mL in 1 BOTTLE (67777-317-03)
467777-317-04236 mL in 1 BOTTLE (67777-317-04)
567777-317-05473 mL in 1 BOTTLE, PUMP (67777-317-05)
667777-317-061.035 mL in 1 PACKET (67777-317-06)
767777-317-071.035 mL in 1 PACKET (67777-317-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67777-317The 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 NAMESannyTize 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 DATE4/25/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDynarex CorporationName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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