NATURAL MINERAL BODY SUNSCREEN

Product NDC
69949-100
11-digit product format
699490100
Labeler code
69949
Product ID
69949-100_63ef5062-4f1d-4f7a-b1a2-88814db88ca3
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 MINERAL BODY SUNSCREEN
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
69949-100-01NATURAL MINERAL BODY SUNSCREEN85 g in 1 TUBECREAM852
69949-100-02NATURAL MINERAL BODY SUNSCREEN141.7 g in 1 TUBECREAM141.72

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69949-100NATURAL MINERAL BODY SUNSCREEN (ZINC OXIDE) CREAM [SYNCHRONICITY SPA, INC. DBA SUNTEGRITY]2Current NDC, Legacy NDC, 2 package rows20241124_dc5116d4-3a42-44d4-b41a-e88b5b16d111.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69949-100-016994901000185 g in 1 TUBE (69949-100-01) 85 g2010-08-120000-00-00NoNoCurrent
69949-100-0269949010002141.7 g in 1 TUBE (69949-100-02) 141.7 g2010-08-120000-00-00NoNoCurrent