SunScreen SPF30

Product NDC
31190-200
11-digit product format
311900200
Labeler code
31190
Product ID
31190-200_9be4854e-39ac-45ca-91d6-d01576baa281
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage form
LOTION
Route
TOPICAL
Labeler
Shanghai Kejing Cleaning Products Co., Ltd.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-04-15
Marketing end
0000-00-00
Substance
HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength
5 mL/100mL; mL/100mL; mL/100mL; mL/100mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
31190-200-102019-10-21C16284748780-1956f9ecf-de36-621f-e053-dbdaa90a74adSunScreen Lotion SPF30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
31190-200-10SunScreen SPF301 in 1 CARTONLOTION14
31190-200-10SunScreen SPF3010 mL in 1 BOTTLE, SPRAYLOTION104

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31190-200SUNSCREEN SPF30 (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [SHANGHAI KEJING CLEANING PRODUCTS CO., LTD.]4Legacy NDC, 2 package rows20100415_d928a1a5-d32a-405d-bac4-20ed54bd8a59.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
31190-200-10311900200101 in 1 CARTONHistorical