Dynamic Sunscreen Broad Spectrum SPF 55 Sun Protection

Product NDC
81693-5550
11-digit product format
816935550
Labeler code
81693
Product ID
81693-5550_bfdf4faa-3cfb-12d1-e053-2a95a90aad40
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate and Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Precision MD Cosmetic Surgery Center
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-01-22
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
75 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81693-5550-32023-01-30C16284748780-1f386c64a-4a1b-0266-e053-dadaa90a7c1aDynamic Sunscreen Broad Spectrum SPF 55 Sun Protection

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81693-5550-3Dynamic Sunscreen Broad Spectrum SPF 55 Sun Protection50 g in 1 BOTTLE, PLASTICCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81693-5550DYNAMIC SUNSCREEN BROAD SPECTRUM SPF 55 SUN PROTECTION (OCTINOXATE AND ZINC OXIDE) CREAM [PRECISION MD COSMETIC SURGERY CENTER]1Legacy NDC, 1 package rows20210414_bfdf5edd-cf58-1cf9-e053-2a95a90a3fd9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81693-5550-38169355500350 g in 1 BOTTLE, PLASTIC (81693-5550-3) 50 g2021-01-220000-00-00NoNoCurrent