All Day Moisture

Product NDC
56062-909
Requested package NDC
56062-909-30
11-digit product format
560620909
Labeler code
56062
Product ID
56062-909_4d1c971d-a441-4e4d-8c6f-a239f1c5be9a
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Publix
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-03-17
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
61 mg/mL; mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage56062-90956062-909-30DDiscontinued by firm2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage56062-90956062-909-30DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage56062-90956062-909-30DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56062-909ALL DAY MOISTURE (OCTINOXATE, ZINC OXIDE) LOTION [PUBLIX]12Legacy NDC20240925_e5293e74-c745-45a0-96bf-60418340e2fb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
56062-909-30560620909301 BOTTLE, PLASTIC in 1 BOX (56062-909-30) > 177 mL in 1 BOTTLE, PLASTIC2016-03-170000-00-00NoNoCurrent