NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER

Product NDC
69949-010
11-digit product format
699490010
Labeler code
69949
Product ID
69949-010_3dc666fa-dd86-4924-9b90-50d240203981
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
2010-08-12
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
NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER
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
69949-010-01NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER50 g in 1 CANISTERCREAM502
69949-010-02NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER50 g in 1 BOXCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69949-010NATURAL MOISTURIZING FACE SUNSCREEN AND PRIMER (ZINC OXIDE) CREAM [SYNCHRONICITY SPA, INC. DBA SUNTEGRITY]2Current NDC, Legacy NDC, 2 package rows20241124_5996f9b2-18c1-4c8f-a0ab-eca180db61ad.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69949-010-016994900100150 g in 1 CANISTER (69949-010-01) 50 g2010-08-120000-00-00NoNoCurrent
69949-010-026994900100250 g in 1 BOX (69949-010-02) 50 g2020-07-010000-00-00NoNoCurrent