Home NDC 59555-102-03 Industrial Strength Sunscreen
Product NDC 59555-102
Requested package NDC 59555-102-03
11-digit product format 595550102
Labeler code 59555
Product ID 59555-102_f68d426e-62ed-4474-b46b-76c23662b331
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Octinoxate, Octisalate, and Oxybenzone
Dosage form LOTION
Route TOPICAL
Labeler R & R Lotion, Inc
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2015-12-21
Marketing end 0000-00-00
Substance ZINC OXIDE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength 64 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 NDC Product Description Form Quantity Strength SPL version 59555-102-01 Industrial Strength Sunscreen 5 mL in 1 PACKET LOTION 5 3 59555-102-03 Industrial Strength Sunscreen 50 mL in 1 BOTTLE, PUMP LOTION 50 3 59555-102-04 Industrial Strength Sunscreen 59 mL in 1 BOTTLE, DISPENSING LOTION 59 3 59555-102-07 Industrial Strength Sunscreen 118 mL in 1 BOTTLE, DISPENSING LOTION 118 3 59555-102-08 Industrial Strength Sunscreen 236 mL in 1 BOTTLE, DISPENSING LOTION 236 3 59555-102-10 Industrial Strength Sunscreen 946 mL in 1 BOTTLE, PUMP LOTION 946 3 59555-102-11 Industrial Strength Sunscreen 3785 mL in 1 BOTTLE, PLASTIC LOTION 3785 3 59555-102-15 Industrial Strength Sunscreen 4 mL in 1 PACKET LOTION 4 3 59555-102-16 Industrial Strength Sunscreen 4 mL in 1 PACKET LOTION 4 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59555-102 INDUSTRIAL STRENGTH SUNSCREEN (ZINC OXIDE, OCTINOXATE, OCTISALATE, AND OXYBENZONE) LOTION [R & R LOTION, INC] 3 Legacy NDC, 9 package rows 20210115_d2e6da66-9c6f-4c7e-b43d-3072e1c6444a.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59555-102-03 59555010203 50 mL in 1 BOTTLE, PUMP (59555-102-03) 50 ml 2015-12-21 0000-00-00 No No Current