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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5b0f43fc-f4a6-4403-a40e-e0198a6f2ebd	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2024-02-13	ALOE UP - PRO SPF 15 SPRAY (61477-207)
2023-07-28	ALOE UP - PRO SPF 15 SPRAY (61477-207)
2022-04-14	ALOE UP - PRO SPF 15 SPRAY (61477-207)
2022-01-28	ALOE UP - PRO SPF 15 SPRAY (61477-207)

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
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 285 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens Broad Spectrum SPF 40 Radiant Facial Sunscreen	AVOBENZONE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	24114416-33b9-c6ba-e063-6394a90a6f3b	2024-10-09	Warnings	Exact identifier application number: M020
Walgreens 40 Invisible Facial Sunscreen Broad Spectrum SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	0c40a46b-b9f9-8e14-e063-6394a90a9573	2024-10-09	Warnings	Exact identifier application number: M020
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.102	ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE	AMOREPACIFIC CORPORATION	531f60c9-c89a-46bc-8460-d01b2e838e6f	2024-10-08	Warnings	Exact identifier application number: M020
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.104	OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE	AMOREPACIFIC CORPORATION	60964d9f-d96c-4397-b273-6b63d1886722	2024-10-08	Warnings	Exact identifier application number: M020
IOPE AIR CUSHION Cover 21 Vanilla	ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE	AMOREPACIFIC CORPORATION	29d6cc8d-1469-479d-a15a-e78d4e22d4a2	2024-10-08	Warnings	Exact identifier application number: M020
IOPE UV DEFENSE SUN PROTECTOR	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	AMOREPACIFIC CORPORATION	0f2a87f7-2185-16a5-e063-6294a90a92a3	2024-10-08	Warnings	Exact identifier application number: M020
Tropical Topical Matte SPF30	ZINC OXIDE	Allure Labs	039fba4b-720a-9199-e063-6394a90adbfb	2024-10-08	Warnings	Exact identifier application number: M020
LANEIGE HYDRO UV DEFENSE EX BROAD SPECTRUM SPF 50	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	AMOREPACIFIC CORPORATION	0e746836-ed84-7b33-e063-6294a90aeff3	2024-10-08	Warnings	Exact identifier application number: M020
DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen	AVOBENZONE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE	PureTek Corporation	86eb06cc-d63f-4500-a52e-14ef99a56532	2024-10-02	Warnings	Exact identifier application number: M020
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	43bec652-3f2c-4671-8a0c-c4c4a4bfcc7a	2024-10-01	Warnings	Exact identifier application number: M020
PROCEUTICALS PRIVATE LABEL by TiZO eye repair non-tinted mineral sunscreen	ZINC OXIDE	Fallien Cosmeceuticals, LTD	231af290-99ee-e94d-e063-6394a90a0bef	2024-09-27	Warnings	Exact identifier application number: M020
Target Up and Up SPF 70 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	TARGET CORPORATION	23085ab9-5abb-a572-e063-6394a90ae34a	2024-09-26	Warnings	Exact identifier application number: M020
Target Up and Up Morning Facial Moisturizing with SPF 30 Sunscreen and Ceramides	HOMOSALATE, OCTOCRYLENE, ZINC OXIDE	TARGET CORPORATION	23598ad1-12a3-fe65-e063-6394a90a4f6f	2024-09-26	Warnings	Exact identifier application number: M020
Target Up and Up SPF 30 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	TARGET CORPORATION	22f59a88-02d7-ebdb-e063-6394a90a957b	2024-09-25	Warnings	Exact identifier application number: M020
Target Up and Up SPF 50 Mineral Zinc Oxide Sunscreen Stick	ZINC OXIDE	TARGET CORPORATION	22f7c376-7289-04bf-e063-6394a90a1459	2024-09-25	Warnings	Exact identifier application number: M020
Target Up and Up SPF 50 Mineral Zinc Oxide Sunscreen	ZINC OXIDE	TARGET CORPORATION	22f86630-d4b4-8ad7-e063-6394a90a8d1e	2024-09-25	Warnings	Exact identifier application number: M020
Target Up and Up SPF 50 Mineral Zinc Oxide Sunscreen	ZINC OXIDE	TARGET CORPORATION	22f9044a-f54c-b34b-e063-6394a90a88ee	2024-09-25	Warnings	Exact identifier application number: M020
BANANA BOAT	AVOBENZONE,HOMOSALATE,OCTISALATE ,OCTOCRYLENE	Edgewell Personal Care Brands LLC	22e2b447-bd6b-5e8a-e063-6394a90a0de9	2024-09-24	Warnings	Exact identifier application number: M020
Luminous Defense SPF 50	ZINC OXIDE	Levels 2 Skin	22e177b3-beea-212e-e063-6394a90a1452	2024-09-24	Warnings	Exact identifier application number: M020
Target Up and Up SPF 50 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	TARGET CORPORATION	22e359cd-4c63-b124-e063-6394a90aec73	2024-09-24	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ALOE UP - PRO SPF 15 SPRAY (61477-207)	Aloe Care International, LLC	2026-01-28	HUMAN OTC DRUG LABEL	10