82735-200 NDC - ONE AND DONE (SPF 40)

Drug Information

  • Product NDC: 82735-200
  • Proprietary Name: One and Done
  • Non Proprietary Name: SPF 40
  • Active Ingredient(s): 2 g/100mL TITANIUM DIOXIDE; 1 g/100mL ZINC OXIDE
  • Administration Route(s): TOPICAL
  • Dosage Form(s): CREAM

Labeler Information

Field Name Field Value
Labeler Name: Thirteen Lune Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:5/30/2022

Package Information

No. Package Code Package Description Billing Unit
182735-200-0150 mL in 1 TUBE (82735-200-01)
282735-200-0215 mL in 1 TUBE (82735-200-02)
382735-200-034 mL in 1 PACKET (82735-200-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82735-200The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEOne and DoneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESPF 40The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/30/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct 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.
APPLICATION NUMBERpart352This 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.
LABELER NAMEThirteen Lune Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETITANIUM DIOXIDE; ZINC OXIDEAn 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.

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This page was last updated on: 4/12/2024