NDC 70359-4106

Poxiezzz

Menthol, Zinc Oxide

Poxiezzz is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Fortunique B.v.. The primary component is Menthol, Unspecified Form; Zinc Oxide.

Product ID70359-4106_43a40622-a711-2d7b-e054-00144ff8d46c
NDC70359-4106
Product TypeHuman Otc Drug
Proprietary NamePoxiezzz
Generic NameMenthol, Zinc Oxide
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2016-01-21
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart347
Labeler NameFortunique B.V.
Substance NameMENTHOL, UNSPECIFIED FORM; ZINC OXIDE
Active Ingredient Strength1 g/100g; g/100g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 70359-4106-1

1 BOTTLE, SPRAY in 1 CARTON (70359-4106-1) > 50 g in 1 BOTTLE, SPRAY
Marketing Start Date2016-01-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70359-4106-1 [70359410601]

Poxiezzz SPRAY
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-21
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MENTHOL, UNSPECIFIED FORM1 g/100g

OpenFDA Data

SPL SET ID:29e1bcc3-3356-591d-e054-00144ff88e88
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1733853