Home NDC 61477-211 ALOE UP PRO 50
Product NDC 61477-211
11-digit product format 614770211
Labeler code 61477
Product ID 61477-211_497ac89a-347f-07c8-e063-6394a90a4f51
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form SPRAY
Route TOPICAL
Labeler Aloe Care International, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-02-24
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength 3; 10; 5; 2.75; 4 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 4 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 2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 61477-211-26 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 61477-211-26 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ALOE UP PRO 50
Brand name suffix CONTINUOUS SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL HOMOSALATE 10 g/100mL OCTISALATE 5 g/100mL OCTOCRYLENE 2.75 g/100mL OXYBENZONE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61477-211-26 ALOE UP PRO 50CONTINUOUS SUNSCREEN 177 mL in 1 CAN SPRAY 177 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded AVOBENZONE ACTIVE INGREDIENT G63QQF2NOX ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 HOMOSALATE ACTIVE INGREDIENT V06SV4M95S ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OCTISALATE ACTIVE INGREDIENT 4X49Y0596W ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OCTOCRYLENE ACTIVE INGREDIENT 5A68WGF6WM ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OXYBENZONE ACTIVE INGREDIENT 95OOS7VE0Y ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 AVOBENZONE ACTIVE MOIETY G63QQF2NOX ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 HOMOSALATE ACTIVE MOIETY V06SV4M95S ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OCTISALATE ACTIVE MOIETY 4X49Y0596W ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OCTOCRYLENE ACTIVE MOIETY 5A68WGF6WM ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 OXYBENZONE ACTIVE MOIETY 95OOS7VE0Y ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 COCONUT OIL INACTIVE INGREDIENT Q9L0O73W7L ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 DIBUTYL MALEATE INACTIVE INGREDIENT 4X371TMK9K ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 DIETHYLHEXYL 2,6-NAPHTHALATE INACTIVE INGREDIENT I0DQJ7YGXM ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 ISOBORNYL METHACRYLATE INACTIVE INGREDIENT 33GSY5DKCQ ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1 POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) INACTIVE INGREDIENT T9296U138P ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61477-211 ALOE UP PRO 50 CONTINUOUS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 5 Current NDC, Legacy NDC, 1 package rows 20240214_dc33d9e8-3463-485d-a1ee-6319ed91454c.zip
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 120 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 387d5194-bc12-68c1-e063-6394a90ab152 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387c23c2-a9f0-f484-e063-6394a90a4104 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387be96f-8cda-ce02-e063-6394a90abea5 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c593b-c65b-62b5-e063-6294a90ac4c2 2025-12-15 Exact identifier application number: M020 Serum Lightly Tinted ZINC OXIDE PANDA PAMPERING LLC 387c9167-638c-1e30-e063-6394a90a9374 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37ede476-43b6-a7c8-e063-6294a90a3e8f 2025-12-15 Exact identifier application number: M020 REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37efa5e1-e88e-d251-e063-6394a90a9371 2025-12-15 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd330bf-92e4-3664-e063-6294a90a0475 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd37dd1-fd43-7af4-e063-6394a90ae3a0 2025-12-15 Warnings Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd3dcab-e9fb-0ef5-e063-6394a90acef1 2025-12-15 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd40a6a-d52e-ab87-e063-6294a90a966e 2025-12-15 Warnings Exact identifier application number: M020 20 Zinc Oxide Non-Tinted Mineral Sunscreen ZINC OXIDE AGELESS SKINCARE INC 3766e6c0-8976-509d-e063-6394a90af00f 2025-12-15 Exact identifier application number: M020 20 Zinc Oxide Tinted Mineral Sunscreen ZINC OXIDE AGELESS SKINCARE INC 3766b00f-ceda-a6f9-e063-6294a90aff5d 2025-12-15 Exact identifier application number: M020 Mattifying Skin Primer TITANIUM DIOXIDE, ZINC OXIDE SKIN MAVEN 37662032-2842-1982-e063-6294a90a49a0 2025-12-15 Exact identifier application number: M020 Moisturizing Face and Body SPF ZINC OXIDE SKIN MAVEN 376645ee-7ea8-e738-e063-6394a90a119b 2025-12-15 Exact identifier application number: M020 Mermaid Glow And Go Non Tinted Mineral Sunscreen ZINC OXIDE Mermaid Glow LLC 3985a298-fe0b-c296-e063-6294a90ab6c0 2025-12-15 Exact identifier application number: M020 Mermaid Glow And Go Non Tinted Mineral Sunscreen ZINC OXIDE Mermaid Glow LLC 39856675-c110-a7a7-e063-6294a90ac6af 2025-12-15 Exact identifier application number: M020 Bio H Plus Daily Defense And Revitalize ZINC OXIDE BIOHEALTH PLUS LLC 3764f723-cc7a-2128-e063-6294a90ac894 2025-12-15 Exact identifier application number: M020 Extreme Protection Non Tinted ZINC OXIDE BIOHEALTH PLUS LLC 37656077-5185-817a-e063-6394a90adf5a 2025-12-15 Exact identifier application number: M020 Deluxe Lip Protection TITANIUM DIOXIDE, ZINC OXIDE BIOHEALTH PLUS LLC 37657895-5fec-82d0-e063-6294a90acf67 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 61477-211-26 61477021126 177 mL in 1 CAN (61477-211-26) 177 ml 2014-02-24 0000-00-00 No No Current