NDC 75936-421 - Best of Glow SPF Discovery Kit

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 75936-421
Package NDCs from labels: 75936-421-01
Manufacturer: Supergoop, LLC
Effective date: 2022-09-29
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Best of Glow SPF Discovery Kit - Supergoop, LLC	Supergoop, LLC	2022-09-29	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75936-421-01	Best of Glow SPF Discovery Kit	30 mL in 1 TUBE	CREAM	15 mL	10 g in 100mL	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75936-421	BEST OF GLOW SPF DISCOVERY KIT (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) KIT [SUPERGOOP, LLC]	1	Unmatched	20221123_e9d86e9f-4409-3f19-e053-2a95a90ac651.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 497 of 497 · 9,924 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Hand Sanitizer	ALCOHOL	CVS	d0081c50-c0d2-436a-ba83-5d1982ae64b7	2015-08-17	Warnings	Exact identifier unii: 3K9958V90M
CVS Sheer SFP 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	CVS Pharmacy	2ea84d12-a5da-41a3-986b-8897f287f00f	2015-07-14	Warnings	Exact identifier unii: 5A68WGF6WM unii: V06SV4M95S unii: G63QQF2NOX unii: 4X49Y0596W
Instant Hand Sanitizer	ALCOHOL	Safetec of America, Inc.	f9e30645-491b-4f54-acfd-f863ee235607	2013-08-07	Warnings	Exact identifier unii: 3K9958V90M
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD.	30468afc-9616-4765-b046-12e97a0a7827	2010-12-20	Warnings	Exact identifier application number: M020

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.