Home NDC 13630-0041 Aloe Up
Product NDC 13630-0041
11-digit product format 136300041
Labeler code 13630
Product ID 13630-0041_9c5be075-dee2-3468-e053-2995a90a6ce6
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate and Oxybenzone
Dosage form SPRAY
Route TOPICAL
Labeler Prime Packaging, Inc.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2009-01-05
Marketing end 0000-00-00
Substance OCTINOXATE; OXYBENZONE
Active strength 17 mg/mL; mg/mL
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 · 30 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 13630-0041-4 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 13630-0041-4 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 13630-0041-4 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 13630-0041-4 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 13630-0041-4 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 13630-0041-4 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 13630-0041-4 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 13630-0041-4 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 13630-0041-4 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 13630-0041-4 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 13630-0041-4 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 13630-0041-4 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 13630-0041-4 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 13630-0041-4 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 13630-0041-4 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 13630-0041-4 Aloe UpDark Tanning Oil SPF 4 177 mL in 1 CAN SPRAY 177 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded OCTINOXATE ACTIVE INGREDIENT 4Y5P7MUD51 ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OXYBENZONE ACTIVE INGREDIENT 95OOS7VE0Y ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OCTINOXATE ACTIVE MOIETY 4Y5P7MUD51 ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OXYBENZONE ACTIVE MOIETY 95OOS7VE0Y ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 ALKYL (C12-15) BENZOATE INACTIVE INGREDIENT A9EJ3J61HQ ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 ASCORBIC ACID INACTIVE INGREDIENT PQ6CK8PD0R ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 CASTOR OIL INACTIVE INGREDIENT D5340Y2I9G ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 COCONUT OIL INACTIVE INGREDIENT Q9L0O73W7L ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 VITAMIN A PALMITATE INACTIVE INGREDIENT 1D1K0N0VVC ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 13630-0041 ALOE UP DARK TANNING OIL SPF 4 (OCTINOXATE AND OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 3 Legacy NDC, 1 package rows 20200118_059a2cf8-924a-44bb-bdf6-0525bb69f49d.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 13630-0041-4 13630004104 177 mL in 1 CAN (13630-0041-4) 177 ml 2009-01-05 0000-00-00 No No Current