Home NDC 65753-102-22 Sun X Multi-Pack SPF 30 Thick
Product NDC 65753-102
Requested package NDC 65753-102-22
11-digit product format 657530102
Labeler code 65753
Product ID 65753-102_98c2882f-3d3d-d96b-e053-2995a90aa491
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
Dosage form LOTION
Route TOPICAL
Labeler CoreTex Products Inc
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-01-01
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength 1 g/100g; g/100g; g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2021-12-31
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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65753-102-22 Sun X Multi-Pack SPF 30 Thick 7 g in 1 POUCH LOTION 7 4 65753-102-22 Sun X Multi-Pack SPF 30 Thick 25 in 1 CONTAINER LOTION 25 4 65753-102-23 Sun X Multi-Pack SPF 30 Thick 25 in 1 CONTAINER LOTION 25 4 65753-102-23 Sun X Multi-Pack SPF 30 Thick 7 g in 1 POUCH LOTION 7 4 65753-102-24 Sun X Multi-Pack SPF 30 Thick 7 g in 1 POUCH LOTION 7 4 65753-102-24 Sun X Multi-Pack SPF 30 Thick 50 in 1 CONTAINER LOTION 50 4 65753-102-26 Sun X Multi-Pack SPF 30 Thick 7 g in 1 POUCH LOTION 7 4 65753-102-26 Sun X Multi-Pack SPF 30 Thick 300 in 1 BOX LOTION 300 4 65753-102-31 Sun X Multi-Pack SPF 30 Thick 150 in 1 BOX LOTION 150 4 65753-102-31 Sun X Multi-Pack SPF 30 Thick 7 g in 1 POUCH LOTION 7 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65753-102 SUN X MULTI-PACK SPF 30 THICK (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [CORETEX PRODUCTS INC] 4 Legacy NDC, 10 package rows 20200228_5ef777a8-67c3-71b9-e053-2991aa0a1cb0.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 65753-102-22 65753010222 25 POUCH in 1 CONTAINER (65753-102-22) > 7 g in 1 POUCH 25 pouch 2017-01-01 0000-00-00 No No Current