42627-102 NDC - ILLUSION LUMINOUS GLOW FOUNDATION (1-26) (AVOBENZONE, HOMOSALATE, AND OCTISALATE)

Drug Information

  • Product NDC: 42627-102
  • Proprietary Name: ILLUSION LUMINOUS GLOW FOUNDATION (1-26)
  • Non Proprietary Name: avobenzone, homosalate, and octisalate
  • Active Ingredient(s): 3 g/100mL AVOBENZONE; 7.34 g/100mL HOMOSALATE; 5 g/100mL OCTISALATE
  • Administration Route(s): TOPICAL
  • Dosage Form(s): LOTION

Labeler Information

Field Name Field Value
Labeler Name: Kingdom Animalia, LLC DBA Hourglass Cosmetics
Product Type: HUMAN OTC DRUG
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:12/1/2024

Package Information

No. Package Code Package Description Billing Unit
142627-102-011 TUBE in 1 CARTON (42627-102-01) / 35 mL in 1 TUBE
242627-102-021 TUBE in 1 CARTON (42627-102-02) / 35 mL in 1 TUBE
342627-102-031 TUBE in 1 CARTON (42627-102-03) / 35 mL in 1 TUBE
442627-102-041 TUBE in 1 CARTON (42627-102-04) / 35 mL in 1 TUBE
542627-102-051 TUBE in 1 CARTON (42627-102-05) / 35 mL in 1 TUBE
642627-102-061 TUBE in 1 CARTON (42627-102-06) / 35 mL in 1 TUBE
742627-102-071 TUBE in 1 CARTON (42627-102-07) / 35 mL in 1 TUBE
842627-102-081 TUBE in 1 CARTON (42627-102-08) / 35 mL in 1 TUBE
942627-102-091 TUBE in 1 CARTON (42627-102-09) / 35 mL in 1 TUBE
1042627-102-101 TUBE in 1 CARTON (42627-102-10) / 35 mL in 1 TUBE
1142627-102-111 TUBE in 1 CARTON (42627-102-11) / 35 mL in 1 TUBE
1242627-102-121 TUBE in 1 CARTON (42627-102-12) / 35 mL in 1 TUBE
1342627-102-131 TUBE in 1 CARTON (42627-102-13) / 35 mL in 1 TUBE
1442627-102-141 TUBE in 1 CARTON (42627-102-14) / 35 mL in 1 TUBE
1542627-102-151 TUBE in 1 CARTON (42627-102-15) / 35 mL in 1 TUBE
1642627-102-161 TUBE in 1 CARTON (42627-102-16) / 35 mL in 1 TUBE
1742627-102-171 TUBE in 1 CARTON (42627-102-17) / 35 mL in 1 TUBE
1842627-102-181 TUBE in 1 CARTON (42627-102-18) / 35 mL in 1 TUBE
1942627-102-191 TUBE in 1 CARTON (42627-102-19) / 35 mL in 1 TUBE
2042627-102-201 TUBE in 1 CARTON (42627-102-20) / 35 mL in 1 TUBE
2142627-102-211 TUBE in 1 CARTON (42627-102-21) / 35 mL in 1 TUBE
2242627-102-221 TUBE in 1 CARTON (42627-102-22) / 35 mL in 1 TUBE
2342627-102-231 TUBE in 1 CARTON (42627-102-23) / 35 mL in 1 TUBE
2442627-102-241 TUBE in 1 CARTON (42627-102-24) / 35 mL in 1 TUBE
2542627-102-251 TUBE in 1 CARTON (42627-102-25) / 35 mL in 1 TUBE
2642627-102-261 TUBE in 1 CARTON (42627-102-26) / 35 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC42627-102The 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 NAMEILLUSION LUMINOUS GLOW FOUNDATION (1-26)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 NAMEavobenzone, homosalate, and octisalateThe 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 DATE12/1/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM020This 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 NAMEKingdom Animalia, LLC DBA Hourglass CosmeticsName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAVOBENZONE; HOMOSALATE; OCTISALATEAn 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 STRENGTH3; 7.34; 5 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL 

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This page was last updated on: 7/4/2025

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