NDC 62932-222 Tinted Mineral Face Sunscreen Stick - Latte

Tinted Mineral Face Sunscreen Stick - Latte

  1. Labeler Index
  2. Private Label Select Ltd Co
  3. NDC: 62932-222 Tinted Mineral Face Sunscreen Stick - Latte

NDC Product Code 62932-222

NDC CODE: 62932-222

Proprietary Name: Tinted Mineral Face Sunscreen Stick - Latte What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Tinted Mineral Face Sunscreen Stick - Latte 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

NDC Code Structure

  • 62932 - Private Label Select Ltd Co
    • 62932-222 - Tinted Mineral Face Sunscreen Stick - Latte

NDC 62932-222-33

Package Description: 14 g in 1 CONTAINER

NDC Product Information

Tinted Mineral Face Sunscreen Stick - Latte with NDC 62932-222 is a a human over the counter drug product labeled by Private Label Select Ltd Co. The generic name of Tinted Mineral Face Sunscreen Stick - Latte is tinted mineral face sunscreen stick - latte. The product's dosage form is stick and is administered via topical form.

Labeler Name: Private Label Select Ltd Co

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

Product Type: Human Otc Drug 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.

Tinted Mineral Face Sunscreen Stick - Latte Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • ZINC OXIDE 20 g/100g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • WHITE WAX (UNII: 7G1J5DA97F)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • .DELTA.-TOCOPHEROL (UNII: JU84X1II0N)
  • COCOA BUTTER (UNII: 512OYT1CRR)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
  • .BETA.-TOCOPHEROL (UNII: 9U6A490501)
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • CASTOR OIL (UNII: D5340Y2I9G)
  • MICA (UNII: V8A1AW0880)
  • .GAMMA.-TOCOPHEROL (UNII: 8EF1Z1238F)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Private Label Select Ltd Co
Labeler Code: 62932
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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.
Start Marketing Date: 12-28-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2021 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.
Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Tinted Mineral Face Sunscreen Stick - Latte Product Label Images