10812-979 NDC - NEUTROGENA OIL FREE MOISTURE BROAD SPECTRUM SPF15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE)

Drug Information

Product NDC: 10812-979

Proprietary Name: Neutrogena Oil Free Moisture Broad Spectrum SPF15

Non Proprietary Name: Avobenzone, Octisalate, Octocrylene, and Oxybenzone

Active Ingredient(s):
  • 15 mg/mL AVOBENZONE;
  • 50 mg/mL OCTISALATE;
  • 30 mg/mL OCTOCRYLENE;
  • 40 mg/mL OXYBENZONE


Administration Route(s): TOPICAL

Dosage Form(s): LOTION

Labeler Information

Labeler Name: Johnson & Johnson Consumer Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:9/15/2014
End Marketing Date:8/23/2023

Package Information

No. Package Code Package Description Billing Unit
110812-979-011 BOTTLE in 1 CARTON (10812-979-01) / 118 mL in 1 BOTTLE
210812-979-0214 mL in 1 TUBE (10812-979-02)
310812-979-0350 mL in 1 TUBE (10812-979-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC10812-979The 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 NAMENeutrogena Oil Free Moisture Broad Spectrum SPF15The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAvobenzone, Octisalate, Octocrylene, and OxybenzoneThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELOTIONThe 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 DATE9/15/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE8/23/2023This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT 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 NAMEJohnson & Johnson Consumer Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONEAn 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.
ACTIVE NUMERATOR STRENGTH15; 50; 30; 40 
ACTIVE INGRED UNITmg/mL; mg/mL; mg/mL; mg/mL 

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This page was last updated on: 2/1/2023