73517-121 NDC - OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE ()

Drug Information

  • Product NDC: 73517-121
  • Proprietary Name: Olika Ultra Hydrating Hand Sanitizer Fragrance Free
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Amyris, Inc
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
173517-121-0190 mL in 1 POUCH (73517-121-01)
273517-121-0230 mL in 1 BOTTLE, DISPENSING (73517-121-02)
373517-121-0320 mL in 1 BOTTLE, DISPENSING (73517-121-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73517-121The 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 NAMEOlika Ultra Hydrating Hand Sanitizer Fragrance FreeIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE3/30/2020The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERpart333AThe translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMEAmyris, IncThis is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 3/6/2026