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OTC products · Product label record

Jack Black Sun Guard Sunscreen SPF45 drug information

SUNSCREEN
Jack Black, LLC · TOPICAL

Product NDC: 66738-304

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSUNSCREEN
Labeler / manufacturerJack Black, LLC
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC66738-304
Label effective date2026-09-08

Official product label reference

Jack Black Sun Guard Sunscreen SPF45 — Jack Black, LLC

This page contains 9 source sections for SUNSCREEN, topical route. Label set 3cc86bb2-05ce-47eb-8c71-f4f116ca5840, version 5.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses Helps prevent sunburn

Purpose

Uses Helps prevent sunburn
Dosage and administration — label text
Directions Apply liberally 15 minutes before sun exposure Reapply: after 80 minutes of swimming or sweating Immediately after towel drying At least every two hours Children under 6 months: ask a doctor Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad spectrum SFP value of 15 or higher Limit time in the sun, eespecially from 10 a.m. - 2 p.m.
Warnings
Warnings For external use only Do not use on damaged or broken skin Stop use and ask doctor if rash occurs When using this product keep out of eyes Rinse with water to remove Keep out of reach of children If swallowed, get medical help or contact Poison Control Cneter right away
Active ingredient
Active Ingredients Octisalate 3.0% Sunscreen Octinoxate 7.5% Sunscreen Zinc Oxide 8.0% Sunscreen
Inactive ingredient
Inactive Ingredients Artemisia Umbelliformis Extract, Ascorbyl Palmitate, Buddleja Davidii Leaf Extract, Butylene Glycol, Calendula Officinalis Flower Extract, Cyclopentasiloxane, Dimethicone, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexyl Isononanoate, Glycerin, Iodopropynyl Butylcarbamate, Lauryl PEG-9 Polymethylsiloxethyl Dimethicone, Leontopodium Aloinum (Edelweiss) Extract, Penoxyethanol, Peucedanum Ostruthium Leaf Extract, Retinyl Palmitate, Sodium Chloride, Triethoxycaprylylsilane, Water
Child safety
KEEP OUT OF REACH OF CHILDREN KEEP OUT OF REACH OF CHILDREN
Other safety information
Other Information Protect product from exessive heat and direct sunlight. You may report a serious adverse reaction from using this product to Jack Black at 1-877-766-3388
Questions
Questions 1-877-766-3388 www.getjackblack.com

Official sources and product identifiers

Substances listed: OCTISALATE, OCTINOXATE, ZINC OXIDE

Package NDC codes

66738-304-14, 66738-304-27

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.