Home NDC 13630-0032 Panama Jack
Product NDC 13630-0032
11-digit product format 136300032
Labeler code 13630
Product ID 13630-0032_e77b6aff-0c43-5a2a-e053-2a95a90a8090
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Dosage form SPRAY
Route TOPICAL
Labeler Prime Packaging, Inc.
Application M020
Marketing category OTC MONOGRAPH FINAL
Marketing start 2012-01-04
Marketing end 2022-12-31
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength 17 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 24 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 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 13630-0032-4 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded AVOBENZONE ACTIVE INGREDIENT G63QQF2NOX PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 HOMOSALATE ACTIVE INGREDIENT V06SV4M95S PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OCTISALATE ACTIVE INGREDIENT 4X49Y0596W PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OCTOCRYLENE ACTIVE INGREDIENT 5A68WGF6WM PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OXYBENZONE ACTIVE INGREDIENT 95OOS7VE0Y PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 AVOBENZONE ACTIVE MOIETY G63QQF2NOX PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 HOMOSALATE ACTIVE MOIETY V06SV4M95S PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OCTISALATE ACTIVE MOIETY 4X49Y0596W PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OCTOCRYLENE ACTIVE MOIETY 5A68WGF6WM PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 OXYBENZONE ACTIVE MOIETY 95OOS7VE0Y PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 DIETHYLHEXYL 2,6-NAPHTHALATE INACTIVE INGREDIENT I0DQJ7YGXM PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1 POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) INACTIVE INGREDIENT T9296U138P PANAMA JACK BROAD SPECTRUM SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [PRIME PACKAGING, INC.] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 121 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bio H Plus Daily Defense And Revitalize ZINC OXIDE BIOHEALTH PLUS LLC 3765331e-ad4b-5661-e063-6294a90a7c20 2025-12-15 Exact identifier application number: M020 Facial Mineral Fusion TITANIUM DIOXIDE, ZINC OXIDE IT INTELLIGENT TREATMENT LLC 35944621-e6fb-cd98-e063-6294a90aa641 2025-12-15 Exact identifier application number: M020 Face Love ZINC OXIDE CLARITY SKIN CARE STUDIO, INC. 35d043a7-7269-469f-e063-6294a90a1a4d 2025-12-15 Exact identifier application number: M020 Mineral Mousse TITANIUM DIOXIDE, ZINC OXIDE CLARITY SKIN CARE STUDIO, INC. 35d00778-3857-ce8f-e063-6394a90ab375 2025-12-15 Exact identifier application number: M020 Chem-Free Sunscreen Non-Tinted Formula ZINC OXIDE IT INTELLIGENT TREATMENT LLC 3594d573-c680-62c9-e063-6294a90a4229 2025-12-15 Exact identifier application number: M020 Chem Free Sunscreen Tinted Formula ZINC OXIDE IT INTELLIGENT TREATMENT LLC 35948531-37ef-1fce-e063-6294a90ae79b 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE R. Sonia Batra, MD, Inc. 35933039-8beb-9f98-e063-6394a90a60bb 2025-12-15 Exact identifier application number: M020 Simply Protected Tinted Mineral Sunscreen ZINC OXIDE Healthy Skin & Body LLC 380416b9-180a-3904-e063-6294a90a7bee 2025-12-15 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE R. Sonia Batra, MD, Inc. 3592edca-cab0-6c44-e063-6294a90a1727 2025-12-15 Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Healthy Skin & Body LLC 38046e71-f171-7e96-e063-6294a90a1f0b 2025-12-15 Exact identifier application number: M020 Barrier Plus Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Healthy Skin & Body LLC 38038beb-d0f0-ced2-e063-6294a90ac423 2025-12-15 Exact identifier application number: M020 Extreme Protection Non Tinted ZINC OXIDE BIOHEALTH PLUS LLC 3764cbeb-55f5-4a9c-e063-6394a90a863d 2025-12-15 Exact identifier application number: M020 Happy Mineral Sunscreen Primer SPF TITANIUM DIOXIDE, ZINC OXIDE ACNE CLINIC LAS VEGAS BY JUSTINA 37d9c5f2-f414-6efa-e063-6294a90a927f 2025-12-15 Exact identifier application number: M020 Comfort Mineral Mousse Sunscreen TITANIUM DIOXIDE, ZINC OXIDE BIOHEALTH PLUS LLC 3765dd17-ffbd-bcf4-e063-6394a90a2c2b 2025-12-15 Exact identifier application number: M020 Prime And Protect Dewy ZINC OXIDE Kalon Skin Studio, LLC 3593cefe-a08f-eb88-e063-6394a90aaff6 2025-12-15 Exact identifier application number: M020 Glow ZINC OXIDE GODDESSLYNNEBODYANDSKIN 37247365-33ee-563d-e063-6394a90a249e 2025-12-15 Exact identifier application number: M020 Prime And Protect Matte TITANIUM DIOXIDE, ZINC OXIDE Kalon Skin Studio, LLC 35939630-1166-1c70-e063-6294a90aac6b 2025-12-15 Exact identifier application number: M020 Non-Tinted 20% Zinc Mineral Sunscreen ZINC OXIDE BELLA MEDICAL SKIN CARE 36d9d83b-7da5-a006-e063-6394a90a9d84 2025-12-15 Exact identifier application number: M020 Non-Tinted 20% Zinc Mineral Sunscreen ZINC OXIDE BELLA MEDICAL SKIN CARE 36da1a55-c076-cdd9-e063-6294a90ac97c 2025-12-15 Exact identifier application number: M020 Tinted Lip Balm TITANIUM DIOXIDE, ZINC OXIDE Goldberg, Howard S MD Inc 3598205d-2e87-9292-e063-6294a90a1f2a 2025-12-15 Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 13630-0032-4 13630003204 177 mL in 1 CAN (13630-0032-4) 177 ml 2012-01-04 0000-00-00 No No Current