5-IN-1 TINTED FACE SUNSCREEN - LIGHT

Product NDC
69949-052
11-digit product format
699490052
Labeler code
69949
Product ID
69949-052_2c5a7500-d9ee-4d1b-b79d-c7adb8e70faf
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Synchronicity Spa, Inc. DBA Suntegrity
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-07-01
Substance
ZINC OXIDE
Active strength
200 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
5-IN-1 TINTED FACE SUNSCREEN - LIGHT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE200 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69949-052-015-IN-1 TINTED FACE SUNSCREEN - LIGHT56.7 g in 1 TUBECREAM56.73

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69949-0525-IN-1 TINTED FACE SUNSCREEN - FAIR (ZINC OXIDE) CREAM 5-IN-1 TINTED FACE SUNSCREEN - LIGHT (ZINC OXIDE) CREAM 5-IN-1 TINTED FACE SUNSCREEN - GOLDEN LIGHT (ZINC OXIDE) CREAM 5-IN-1 TINTED FACE SUNSCREEN - MEDIUM (ZINC OXIDE) CREAM [SYNCHRONICITY SPA, INC. DBA SUNTEGRITY]2Current NDC, Legacy NDC, 1 package rows20241124_c0892856-cd12-4c1f-8420-866dbd0f8907.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69949-052-016994900520156.7 g in 1 TUBE (69949-052-01) 56.7 g2013-07-010000-00-00NoNoCurrent