Jack Black The Supreme Shave

Manufacturer
Jack Black L.L.C | Swiss American CDMO
Effective date
2024-04-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:04:33

Label at a glance#

ProductJack Black The Supreme Shave
Active ingredientAVOBENZONE, OCTINOXATE
Label structure13 sections

Dosage and administration

Apply liberally after cleansing and shaving and 15 minutes before sun exposure. • Use a water-resistant sunscreen if swimming or sweating. • Reapply at least every two hours. • Children under 6 months : Ask a doctor. Sun Protection Measures • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, use sunscreen with a broad spectrum SPF 15 or higher. • Limit time in...

Storage and handling

• Protect product from excessive heat and direct sunlight • You may report a serious adverse reaction from using this product to Jack Black at 1-877-766-3388.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.2%

Octinoxate 7.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Moisturizes and helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - STOP USE SECTION

Stop use and ask doctor if rash occurs.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

• If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally after cleansing and shaving and 15 minutes before sun exposure. • Use a water-resistant sunscreen if swimming or sweating. • Reapply at least every two hours. • Children under 6 months: Ask a doctor. Sun Protection Measures • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, use sunscreen with a broad spectrum SPF 15 or higher. • Limit time in the sun, especially from 10 a.m. – 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavandula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis Extract, Haslea Ostrearia Extract, Palmaria Palmata Extract, Calendula Officinalis Flower Extract*, Glycerin, Leontopodium Alpinum (Edelweiss) Extract*, Retinyl Palmitate, Tocopheryl Acetate, Anthemis Nobilis Flower Oil, Peucedanum Ostruthium Leaf Extract*, Buddleja Davidii Leaf Extract*, Artemisia Umbelliformis Extract*.

* Certified Organic

Other Information

STORAGE AND HANDLING SECTION

• Protect product from excessive heat and direct sunlight • You may report a serious adverse reaction from using this product to Jack Black at 1-877-766-3388.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Double DutyDouble Duty

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66738-631-402024-04-23C16284748780-1f386c649-e11f-0266-e053-dadaa90a7c1ab08f0804-9946-8668-e053-2a95a90a4a42
66738-631-402023-01-30C16284748780-1f386c649-e11f-0266-e053-dadaa90a7c1ab08f0804-9946-8668-e053-2a95a90a4a42

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66738-63166738-631-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
16c91e78-840a-b143-e063-6394a90a745bb08f0804-9946-8668-e053-2a95a90a4a422024-04-23WarningsExact identifier
spl id: 16c91e78-840a-b143-e063-6394a90a745b
spl set id: b08f0804-9946-8668-e053-2a95a90a4a42

Reported adverse events (FAERS/openFDA)#

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