ALOE UP LIGHT TANNING OIL

Product NDC
61477-226
Requested package NDC
61477-226-24
11-digit product format
614770226
Labeler code
61477
Product ID
61477-226_dc94971d-133e-9018-e053-2a95a90ad2b2
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, OCTYL SALICYLATE, HOMOSALATE, OCTOCRYLENE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Aloe Care International, LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-05-17
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
1 g/100mL; g/100mL; g/100mL; g/100mL
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 packagepackage61477-22661477-226-24IInactivated by FDA2026-10-05

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
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage61477-22661477-226-24IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage61477-22661477-226-24IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61477-226-24ALOE UP LIGHT TANNING OILSPF-6120 mL in 1 BOTTLE, SPRAYSPRAY1205

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61477-226ALOE UP LIGHT TANNING OIL SPF-6 (AVOBENZONE, OCTYL SALICYLATE, HOMOSALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC]5Legacy NDC, 1 package rows20240214_c65cb736-a82f-4df5-ae53-1a40092c41f5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61477-226-2461477022624120 mL in 1 BOTTLE, SPRAY (61477-226-24) 120 ml2019-05-170000-00-00NoNoCurrent