Home NDC 61477-207 ALOE UP PRO 15
Product NDC 61477-207
11-digit product format 614770207
Labeler code 61477
Product ID 61477-207_497ac89a-347e-07c8-e063-6394a90a4f51
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, OCTISALATE, OCTOCRYLENE
Dosage form SPRAY
Route TOPICAL
Labeler Aloe Care International, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-02-24
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Active strength 2; 5; 1.85 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 61477-207-16 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 61477-207-16 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 15
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 2 g/100mL OCTISALATE 5 g/100mL OCTOCRYLENE 1.85 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
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 61477-207-16 ALOE UP PRO 15 177 mL in 1 BOTTLE, SPRAY SPRAY 177 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded AVOBENZONE ACTIVE INGREDIENT G63QQF2NOX ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 OCTISALATE ACTIVE INGREDIENT 4X49Y0596W ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 OCTOCRYLENE ACTIVE INGREDIENT 5A68WGF6WM ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 AVOBENZONE ACTIVE MOIETY G63QQF2NOX ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 OCTISALATE ACTIVE MOIETY 4X49Y0596W ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 OCTOCRYLENE ACTIVE MOIETY 5A68WGF6WM ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 COCONUT OIL INACTIVE INGREDIENT Q9L0O73W7L ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 DIBUTYL MALEATE INACTIVE INGREDIENT 4X371TMK9K ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 DIETHYLHEXYL 2,6-NAPHTHALATE INACTIVE INGREDIENT I0DQJ7YGXM ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 ISOBORNYL METHACRYLATE INACTIVE INGREDIENT 33GSY5DKCQ ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3 POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) INACTIVE INGREDIENT T9296U138P ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61477-207 ALOE UP PRO 15 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) SPRAY [ALOE CARE INTERNATIONAL, LLC] 9 Current NDC, Legacy NDC, 1 package rows 20240214_5b0f43fc-f4a6-4403-a40e-e0198a6f2ebd.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 118 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Non Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 39959db9-5ee1-a27c-e063-6394a90a1e10 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3995f556-20fe-3e64-e063-6294a90a5efe 2025-12-15 Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3995385b-b10b-ca5c-e063-6294a90af43f 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3994aa84-30b4-3dc4-e063-6394a90a23e7 2025-12-15 Exact identifier application number: M020 Non Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 39947913-f1cc-25d2-e063-6294a90a4229 2025-12-15 Exact identifier application number: M020 Non Tinted Mineral Sunscreen ZINC OXIDE Micro Fibro Blast 35425e24-3e2c-51db-e063-6394a90a5580 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted ZINC OXIDE DENISE BELL SKIN CARE 396fe2ca-eb29-5952-e063-6294a90ab279 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f91b3-3326-3239-e063-6294a90a5df9 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE Micro Fibro Blast 35422370-eb55-049c-e063-6294a90ad0a4 2025-12-15 Exact identifier application number: M020 Eclipse Face Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f0151-2d0d-f4da-e063-6394a90a5f7f 2025-12-15 Exact identifier application number: M020 Eclipse Body Non Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f56df-d0de-1344-e063-6294a90a46ea 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted TITANIUM DIOXIDE, ZINC OXIDE DENISE BELL SKIN CARE 396eb781-5947-3665-e063-6294a90a38dd 2025-12-15 Exact identifier application number: M020 Sun Veil Illuminating Sunscreen SPF30 ZINC OXIDE Koco Life LLC 46001097-540e-65da-e063-6294a90af299 2025-12-15 Warnings Exact identifier application number: M020 Mineral Primer tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 3542d8d3-35a3-7d63-e063-6394a90a6fd1 2025-12-15 Exact identifier application number: M020 Mineral Primer non-tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 354357de-1a85-3bdb-e063-6294a90aa9a2 2025-12-15 Exact identifier application number: M020 Mineral Primer tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 35433254-1dc8-a8f3-e063-6394a90a29f0 2025-12-15 Exact identifier application number: M020 Sun Therapy Sunscreen ZINC OXIDE Skin Therapy Studio LLC 3544916b-3f63-3a7a-e063-6394a90ae507 2025-12-15 Exact identifier application number: M020 Ultra Zinc Mineral Non Tinted ZINC OXIDE Skin Therapy Studio LLC 3545d603-3d01-c51d-e063-6394a90a1599 2025-12-15 Exact identifier application number: M020 Sun Therapy Sunscreen ZINC OXIDE Skin Therapy Studio LLC 357efafb-aa1c-0d69-e063-6394a90a5135 2025-12-15 Exact identifier application number: M020 Ultra Zinc Mineral Non Tinted ZINC OXIDE Skin Therapy Studio LLC 35806102-6919-116f-e063-6294a90ad922 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 61477-207-16 61477020716 177 mL in 1 BOTTLE, SPRAY (61477-207-16) 177 ml 2014-02-24 0000-00-00 No No Current