Parasol Daily Mineral Sunscreen

Product NDC
85373-208
11-digit product format
853730208
Labeler code
85373
Product ID
85373-208_46044770-a650-78d2-e063-6294a90afbc4
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Bodi & Wax, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-05-05
Substance
ZINC OXIDE
Active strength
160 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Parasol Daily Mineral Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE160 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85373-208-15Parasol Daily Mineral Sunscreen1.5 g in 1 PACKETCREAM1.52
85373-208-50Parasol Daily Mineral Sunscreen50 g in 1 BOTTLE, PUMPCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85373-208PARASOL DAILY MINERAL SUNSCREEN (ZINC OXIDE) CREAM [BODI & WAX, LLC]1Current NDC, 1 package rows20250525_35d2fbeb-935b-f0a9-e063-6294a90acd79.zip
85373-208PARASOL DAILY MINERAL SUNSCREEN (ZINC OXIDE) CREAM [BODI & WAX, LLC]1Current NDC, 1 package rows20250525_35d3262a-1d8d-2afa-e063-6294a90afd49.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85373-208-15853730208151.5 g in 1 PACKET (85373-208-15) 1.5 g2025-05-05YesNoHistorical
85373-208-508537302085050 g in 1 BOTTLE, PUMP (85373-208-50) 50 g2025-05-05NoNoHistorical