13630-0166 NDC - EVERYMAN JACK ()

Drug Information

  • Product NDC: 13630-0166
  • Proprietary Name: Everyman Jack
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Prime Packaging, Inc.
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:6/12/2020

Package Information

No. Package Code Package Description Billing Unit
113630-0166-4170 g in 1 CAN (13630-0166-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC13630-0166The 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.
PROPRIETARY NAMEEveryman JackIndicates 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 SUFFIXBroad Spectrum SPF 50The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/12/2020The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the 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 NAMEPrime Packaging, Inc.This is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 11/21/2025

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