Presidents Choice

Manufacturer: Fruit of the Earth, Inc.
Effective date: 2010-04-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:24:17

Label at a glance#

ProductPresidents Choice

Active ingredientOctinoxate, Homosalate, Oxybenzone, Avobenzone

Label structure5 sections

Dosage and administration

Enter section text here Apply liberally 15 to 30 minutes before sun exposure. Reapply after swimming, excessive perspiration or washing. The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years may reduce the chance of these harmful effects.

Label contents#

Full prescribing information#

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Enter section text here

President's Choice SPF/FPS 30 Sunblock Lotion

Broadspectrum UVA/UVB Protection

Non-comedogenic

Dermatologist tested

Waterproof

220 mL

Recognized by the Canadian Dermatology Association

DIN # 02263068

Directions

DOSAGE & ADMINISTRATION SECTION

Enter section text here

Apply liberally 15 to 30 minutes before sun exposure. Reapply after swimming, excessive perspiration or washing.

The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years may reduce the chance of these harmful effects.

CAUTION

GENERAL PRECAUTIONS SECTION

Enter section text here

CAUTION: FOR EXTERNAL USE ONLY. DISCONTINUE USE IF SIGNS OF RASH OR IRRITATION DEVELOP. AVOID CONTACT WITH EYES. FOR USE ON CHILDREN UNDER 6 MONTHS OF AGE, CONSULT YOUR DOCTOR. MINIMIZE YOUR CHILD'S EXPOSURE TO THE SUN; DRESS BABIES AND YOUNG CHILDREN IN APPROPRIATE PROTECTIVE CLOTHING. KEEP OUT OF THE REACH OF CHILDREN.

Medicinal Ingredients

OTC - ACTIVE INGREDIENT SECTION

Enter section text here

MEDICINAL INGREDIENTS: OCTINOXATE (7.5%), HOMOSALATE (5%), OXYBENZONE (4%), AVOBENZONE (2%)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of product label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62217-152-23	2019-10-21	C162847	48780-1	956f9ecf-dc92-621f-e053-dbdaa90a74ad	f7c4869b-d68d-423c-94cf-221ffa5e7f4d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62217-152-23	Presidents Choice	220 g in 1 TUBE	LOTION	220		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62217-152	PRESIDENTS CHOICE (OCTINOXATE, HOMOSALATE, OXYBENZONE, AVOBENZONE) LOTION [FRUIT OF THE EARTH, INC.]	2	Legacy NDC, 1 package rows	20100420_f7c4869b-d68d-423c-94cf-221ffa5e7f4d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Avobenzone	ACTIVE INGREDIENT	G63QQF2NOX	2
Homosalate	ACTIVE INGREDIENT	V06SV4M95S	2
Octinoxate	ACTIVE INGREDIENT	4Y5P7MUD51	2
Oxybenzone	ACTIVE INGREDIENT	95OOS7VE0Y	2
Avobenzone	ACTIVE MOIETY	G63QQF2NOX	2
Homosalate	ACTIVE MOIETY	V06SV4M95S	2
Octinoxate	ACTIVE MOIETY	4Y5P7MUD51	2
Oxybenzone	ACTIVE MOIETY	95OOS7VE0Y	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Presidents Choice
Octinoxate, Homosalate, Oxybenzone, Avobenzone
Octinoxate
Homosalate
Oxybenzone
Avobenzone

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62217-152	62217-152-23

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Octinoxate	4Y5P7MUD51	ACTIB
Homosalate	V06SV4M95S	ACTIB
Oxybenzone	95OOS7VE0Y	ACTIB
Avobenzone	G63QQF2NOX	ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
e7f02de2-e352-45ee-9136-5b21952326d6			f7c4869b-d68d-423c-94cf-221ffa5e7f4d	2010-04-06		Exact identifier spl id: e7f02de2-e352-45ee-9136-5b21952326d6 spl set id: f7c4869b-d68d-423c-94cf-221ffa5e7f4d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.