Menow Sunscreen Powder
NDC 85138-101

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 85138-101?
  4. Menow Sunscreen Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Menow Sunscreen (ethylhexyl methoxycinnamate, bis-ethylhexyloxyphenol methoxyphenyl triazine, zinc oxide, titanium dioxide) is a UNAPPROVED DRUG OTHER-approved product labeled by Shantou Qiwei Industry Co.,ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a powder for cutaneous administration. This product entry covers the primary NDC 85138-101 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
85138-101
Proprietary Name:
Menow Sunscreen
Non-Proprietary Name: [1]
Ethylhexyl Methoxycinnamate, Bis-ethylhexyloxyphenol Methoxyphenyl Triazine, Zinc Oxide, Titanium Dioxide
Substance Name: [2]
Bis-ethylhexyloxyphenol Methoxyphenyl Triazine; Ethylhexyl Methoxycinnamate; Titanium Dioxide; Zinc Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s): [4]
Cutaneous - Administration to the skin.

Labeler & Regulatory Data

Labeler Name: [5]
Shantou Qiwei Industry Co.,ltd
Labeler Code:
85138
Product Label ID:
2be1dfce-1881-aab3-e063-6394a90ac464
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
01-17-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 85138-101?

The NDC code 85138-101 is assigned by the FDA to the product Menow Sunscreen. It is commonly known by its generic name, ethylhexyl methoxycinnamate, bis-ethylhexyloxyphenol methoxyphenyl triazine, zinc oxide, titanium dioxide. This pharmaceutical product is labeled by Shantou Qiwei Industry Co.,ltd and is currently categorized as listed product. The medication is a powder administered via cutaneous route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 85138-101-02. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Indications & usage section:SUNSCREEN PRESSED POWDER,SETTING MAKEUP WHILE PROTECTING AGAINST UVA/UVB

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE (UNII: PWZ1720CBH)
  • BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE (UNII: PWZ1720CBH) (Active Moiety)
  • ZINC OXIDE (UNII: SOI2LOH54Z)
  • ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
  • ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)
  • ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (Active Moiety)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".