75682-849 NDC - SANTATIZER HAND SANITIZER GEL ()

Drug Information

Product NDC: 75682-849

Proprietary Name: SANTAtizer Hand Sanitizer Gel

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Froggy's Fog LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
175682-849-013785.412 mL in 1 JUG (75682-849-01)
275682-849-0259.14 mL in 1 BOTTLE, PLASTIC (75682-849-02)
375682-849-04118.284 mL in 1 BOTTLE, PLASTIC (75682-849-04)
475682-849-08236 mL in 1 BOTTLE, PLASTIC (75682-849-08)
575682-849-16473.176 mL in 1 BOTTLE, PLASTIC (75682-849-16)
675682-849-32946.353 mL in 1 BOTTLE, PLASTIC (75682-849-32)
775682-849-331000 mL in 1 JUG (75682-849-33)
875682-849-641892.71 mL in 1 JUG (75682-849-64)
975682-849-672000 mL in 1 JUG (75682-849-67)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75682-849The 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 NAMESANTAtizer Hand Sanitizer GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFroggy's Fog LLCName 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