PORESCREEN SPF40

Product NDC
68479-291
11-digit product format
684790291
Labeler code
68479
Product ID
68479-291_67812343-d9bc-43df-88d2-85adf578604e
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Dermalogica, LLC.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-01
Substance
ZINC OXIDE
Active strength
10 mg/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PORESCREEN SPF40
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE10 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68479-291-02PORESCREEN SPF4030 mL in 1 TUBELOTION304
68479-291-02PORESCREEN SPF401 in 1 CARTONLOTION14
68479-291-04PORESCREEN SPF4059 mL in 1 TUBELOTION594
68479-291-05PORESCREEN SPF405 mL in 1 TUBELOTION54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68479-291PORESCREEN SPF40 (ZINC OXIDE) LOTION [DERMALOGICA, LLC.]4Current NDC, Legacy NDC, 4 package rows20250101_37a7362a-b251-4d3a-a957-65d8f338fa12.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68479-291-02684790291021 TUBE in 1 CARTON (68479-291-02) / 30 mL in 1 TUBE1 tube2022-12-010000-00-00NoNoCurrent
68479-291-046847902910459 mL in 1 TUBE (68479-291-04) 59 ml2022-12-010000-00-00NoNoCurrent
68479-291-05684790291055 mL in 1 TUBE (68479-291-05) 5 ml2022-12-010000-00-00NoNoCurrent