TONE UP WHITE SUN

Product NDC
69894-310
11-digit product format
698940310
Labeler code
69894
Product ID
69894-310_a61342ff-6a0f-4604-8e4c-143a8d574313
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide, Titanium Dioxide, Octinoxate, Octisalate
Dosage form
CREAM
Route
TOPICAL
Labeler
WOW VENTURES
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-05-01
Marketing end
0000-00-00
Substance
ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE; OCTISALATE
Active strength
4 mg/50mL; mg/50mL; mg/50mL; mg/50mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69894-310-012020-01-31C16284748780-19d75b9d0-4666-f424-e053-dadaa90a57ce85759f43-2903-48ff-939e-46f9661a1613

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69894-310-01TONE UP WHITE SUN50 mL in 1 CARTONCREAM501

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69894-310TONE UP WHITE SUN (ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) CREAM [WOW VENTURES]1Legacy NDC, 1 package rows20150626_85759f43-2903-48ff-939e-46f9661a1613.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69894-310-016989403100150 mL in 1 CARTON50 mlHistorical