MyChelle Dermaceuticals Sun Shield SPF 50 Non-Tinted

Product NDC
72805-081
11-digit product format
728050081
Labeler code
72805
Product ID
72805-081_30640f8f-4284-4daa-b0a9-427ecd3ffbe5
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LIQUID
Route
TOPICAL
Labeler
French Transit, Ltd.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-03-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
21 g/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72805-081-312024-01-30C16284748780-11030e365-0ecd-111a-e063-dadaa90a10e2MyChelle ® Dermaceuticals Sun Shield Liquid SPF 50 Non-Tinted Protect

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72805-081-31MyChelle Dermaceuticals Sun Shield SPF 50 Non-Tinted Protect30 mL in 1 BOTTLE, DROPPERLIQUID302
72805-081-31MyChelle Dermaceuticals Sun Shield SPF 50 Non-Tinted Protect1 in 1 BOXLIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72805-081MYCHELLE DERMACEUTICALS SUN SHIELD SPF 50 NON-TINTED PROTECT (ZINC OXIDE) LIQUID [FRENCH TRANSIT, LTD.]2Legacy NDC, 2 package rows20220108_4f7a1550-73e1-435c-b481-14cb20cabc51.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72805-081-31728050081311 BOTTLE, DROPPER in 1 BOX (72805-081-31) > 30 mL in 1 BOTTLE, DROPPER2020-03-010000-00-00NoNoCurrent