Odacite Flex Perfecting Mineral Drops Tinted Sunscreen

Product NDC
82088-214
11-digit product format
820880214
Labeler code
82088
Product ID
82088-214_52553a25-7d0c-42ce-e063-6294a90af882
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Odacite
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-09-21
Substance
ZINC OXIDE
Active strength
132 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Odacite Flex Perfecting Mineral Drops Tinted Sunscreen
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE132 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82088-214-01Odacite Flex Perfecting Mineral Drops Tinted Sunscreen30 mL in 1 BOTTLE, GLASSLOTION301
82088-214-02Odacite Flex Perfecting Mineral Drops Tinted Sunscreen1 in 1 CARTONLOTION11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82088-214-018208802140130 mL in 1 BOTTLE, GLASS30 mlHistorical
82088-214-02820880214021 BOTTLE, GLASS in 1 CARTON (82088-214-02) / 30 mL in 1 BOTTLE, GLASS (82088-214-01) 2023-09-21NoNoHistorical