PHYSIOGEL Daily Moisture Therapy Barrier Mineral Sunscreen Broad Spectrum SPF 50

Product NDC
53208-251
11-digit product format
532080251
Labeler code
53208
Product ID
53208-251_14101233-f429-bd95-e063-6294a90a8691
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
LG H&H Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-18
Substance
ZINC OXIDE
Active strength
15.52 g/50mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PHYSIOGEL Daily Moisture Therapy Barrier Mineral Sunscreen Broad Spectrum SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE15.52 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53208-251-50PHYSIOGEL Daily Moisture Therapy Barrier Mineral Sunscreen Broad Spectrum SPF 501 in 1 BOXCREAM11
53208-251-50PHYSIOGEL Daily Moisture Therapy Barrier Mineral Sunscreen Broad Spectrum SPF 5050 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53208-251PHYSIOGEL DAILY MOISTURE THERAPY BARRIER MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 (ZINC OXIDE) CREAM [LG H&H CO., LTD.]1Current NDC, 2 package rows20240321_140feb1e-a72f-ade4-e063-6394a90a11fb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
53208-251-50532080251501 TUBE in 1 BOX (53208-251-50) / 50 mL in 1 TUBE1 tube2024-03-18NoNoCurrent