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 281 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join H.E.B. Mineral Sunscreen Broad Spectrum SPF 50 TITANIUM DIOXIDE, ZINC OXIDE H.E.B. c5279caf-3af9-d163-e053-2995a90a943b 2024-10-15 Warnings Exact identifier application number: M020 HEB Face 50 Clear Zinc Sunscreen OCTOCRYLENE, ZINC OXIDE H.E.B. f6e3c883-0087-dcd6-e053-6394a90a1272 2024-10-15 Warnings Exact identifier application number: M020 HEB Mineral Sunscreen SPF 50 ZINC OXIDE H.E.B. de99343b-c74c-3f43-e053-2995a90ac9dd 2024-10-15 Warnings Exact identifier application number: M020 HEB SPF 55 Babies and Kids Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B. f5660a97-57c8-61c7-e053-2995a90a0164 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 362f726b-d52b-4dae-ade6-a47de47697ef 2024-10-15 Warnings Exact identifier application number: M020 HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face ZINC OXIDE H.E.B. dfb43fc5-4968-f999-e053-2a95a90a0819 2024-10-15 Warnings Exact identifier application number: M020 H.E.B BABY SPF 50 SUNSCREEN H.E.B 61273611-ab7a-4216-aebe-2c8d89660281 2024-10-15 Warnings Exact identifier application number: M020 H.E.B BANANA SPF 50 SUNSCREEN H.E.B b9a9837a-094b-4a57-a50c-5c1437deda7b 2024-10-15 Warnings Exact identifier application number: M020 HEB Solutions Sunscreen SPORT SPF 100 LOTION H.E.B 9e3ea66c-d6a0-49ca-a3c0-8175e0617453 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 LOTION H.E.B 12c76c72-4411-48d5-b79b-c58703bf1fdd 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 50 CONTINUOUS SPRAY H.E.B 86ad5d30-f700-42a2-b810-dd2e3ed0f2d8 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 1f8d4f91-9eb9-41de-9066-a7a08c7ff84f 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 100 CONTINUOUS SPRAY H.E.B be80244d-da6d-4d37-b228-4d3fac335caf 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen KIDS SPF 50 LOTION SPRAY H.E.B 9b43c5d5-c279-4ae3-843e-1451f7324216 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 2e183ba8-1b83-4211-bc08-dbdcee942ce9 2024-10-15 Warnings Exact identifier application number: M020 EQUALINE KIDS SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE United Natural Foods, Inc. dba UNFI e46cb6e3-ea8d-3c2d-e053-2a95a90a0bf6 2024-10-15 Warnings Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE SUNSCREEN Bentley Laboratories LLC 782a8641-7e6a-413b-a2ed-0efeb36c48a7 2024-10-15 Warnings Exact identifier application number: M020 H.E.B MANGO SPF 50 SUNSCREEN H.E.B 35898f07-2973-461a-91b8-095aa4cf38ee 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 30 CONTINUOUS SPRAY H.E.B 8b6d0c0d-485b-4428-91e5-5befcac18d5d 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 5fd3d730-d916-48f4-bb94-62d40d181280 2024-10-15 Warnings 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