MyChelle Dermaceuticals Sun Shield Non-Tinted

Product NDC
72805-080
11-digit product format
728050080
Labeler code
72805
Product ID
72805-080_2389b220-ff07-487c-88f3-84a4ea1e024c
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
2017-11-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
21 g/100mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72805-080-30MyChelle Dermaceuticals Sun Shield Non-Tinted SPF 50 Broad Spectrum30 mL in 1 BOTTLE, PUMPLIQUID303
72805-080-30MyChelle Dermaceuticals Sun Shield Non-Tinted SPF 50 Broad Spectrum1 in 1 BOXLIQUID13
72805-080-31MyChelle Dermaceuticals Sun Shield Non-Tinted SPF 50 Broad Spectrum1 in 1 BOXLIQUID13
72805-080-31MyChelle Dermaceuticals Sun Shield Non-Tinted SPF 50 Broad Spectrum30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72805-080MYCHELLE DERMACEUTICALS SUN SHIELD NON-TINTED SPF 50 BROAD SPECTRUM (ZINC OXIDE) LIQUID [FRENCH TRANSIT, LTD.]3Legacy NDC, 4 package rows20190910_d52ecb43-01f2-437e-be10-b7681ea81687.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
72805-080-307280500803030 mL in 1 BOTTLE, PUMP30 mlHistorical
72805-080-31728050080311 in 1 BOXHistorical