62217-186 NDC - FRUIT OF THE EARTH BLOCK UP (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)

Drug Information

Product NDC: 62217-186
Proprietary Name: Fruit of the Earth Block Up
Non Proprietary Name: Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone
Active Ingredient(s): 20 mg/mL AVOBENZONE; 90 mg/mL HOMOSALATE; 75 mg/mL OCTINOXATE; 50 mg/mL OCTISALATE; 15 mg/mL OCTOCRYLENE; 50 mg/mL OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION

Labeler Information

Field Name	Field Value
Labeler Name:	FRUIT OF THE EARTH, INC.
Product Type:	HUMAN OTC DRUG
FDA Application Number:	M020
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	8/24/2011
End Marketing Date:	7/7/2025

Package Information

No.	Package Code	Package Description	Billing Unit
1	62217-186-12	237 mL in 1 TUBE (62217-186-12)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	62217-186	The 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 NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	Fruit of the Earth Block Up	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Broad Spectrum Sport SPF 50	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAME	Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LOTION	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	8/24/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	7/7/2025	This 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 NAME	OTC MONOGRAPH DRUG	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.
APPLICATION NUMBER	M020	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.
LABELER NAME	FRUIT OF THE EARTH, INC.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE	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.
ACTIVE NUMERATOR STRENGTH	20; 90; 75; 50; 15; 50
ACTIVE INGRED UNIT	mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

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This page was last updated on: 5/9/2025

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