Plius Daily SPF Moisturizer SPF 30

Product NDC
80573-089
11-digit product format
805730089
Labeler code
80573
Product ID
80573-089_48c0c6c7-dfa3-d42d-e063-6394a90a024e
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form
CREAM
Route
TOPICAL
Labeler
PLIUS, Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-14
Substance
AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength
30; 50; 80 mg/mL; mg/mL; 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
Plius Daily SPF Moisturizer SPF 30
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE80 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80573-089-30Plius Daily SPF Moisturizer SPF 301 in 1 CARTONCREAM14
80573-089-30Plius Daily SPF Moisturizer SPF 3030 mL in 1 TUBECREAM304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80573-089PLIUS DAILY SPF MOISTURIZER SPF 30 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) CREAM [PLIUS, INC]3Current NDC, Legacy NDC, 2 package rows20231106_31866de9-afa0-4c11-be65-b61373551493.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80573-089-30805730089301 TUBE in 1 CARTON (80573-089-30) / 30 mL in 1 TUBE1 tube2020-09-140000-00-00NoNoCurrent