Super Power Sunscreen Mousse SPF 50

Manufacturer
TAYLOR JAMES, LTD. | Chemolee Lab Corporation
Effective date
2017-01-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:40

Label at a glance#

ProductSuper Power Sunscreen Mousse SPF 50 Supergoop
Active ingredientAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredients                  Purpose

Avobenzone 3% ....................... Sunscreen

Homosalate 10% ...................... Sunscreen

Octinoxate 7.5% ....................... Sunscreen

Octisalate 5% ........................... Sunscreen

OTC - PURPOSE SECTION

​Uses

Helps prevent sunburn

  • If used as directed with other sun protection measures (see Direction), decreases the risk of skin cancer and early skin aging caused by the sun

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs

WARNINGS SECTION

​Warnings

For external use only

  • Do not use on damaged or broken skin
  • When using this product keep out of eyes
  • Rinse with water to remove
  • If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

​Directions

  • Apply liberally 15 minutes before sun exposure
  • Reapply after 80 minutes of swimming or sweating
  • Immediately after towel drying
  • At least every 2 hours
  • Children under 6 months: Ask a doctor

​Sun Protection Measures ​Spending time in teh sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: 

  • Limit time in the sun, especially from 10 a.m. - 2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENT SECTION

Aluminum Starch Octenylsuccinate, Ananas Sativus (Pineapple) Fuit Extract, Bis-Hydroxyethoxypropyl Dimethicone, Butter Extract, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Cananga Odorata Flower Extract, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Chlorphenesin, Citrus Aurantium Dulcis (Orange) Peel Extract, Citrus Grandis (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Peel Extract, Cocos Nucifera (Cocnut) Fruit Extract, Cocos Nucifera (Coconut) Oil, Arabica (Coffee) Seed Extract, Crambe Maritima Leaf Extract, Cucumis Melo Cantalupensis Fruit Extract, Cucumis Sativus (Cucumber) Fruit Extract, Diethylhexyl Syringylidenemalonate, Disodium EDTA, Glycerin, Glyceryl Caprylate, Glyceryl Stearate, Glyceryl Undecylenate, Hydrofluorocarbon 152A, Olea Europaea (Olive) Fruit Oil, Panthenol, Passiflora Incarnata Fruit Extract, Persea Gratissima (Avocado) Oil, Polyester-5, Potassium Cetyl Phosphate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Prunus Amygdalus Dulcis (Sweet Almond) Seed Extract, Prunus Armeniaca (Apricot) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Rose Extract, Rubus Idaeus (Raspberry) Fruit Extract, Santalum Album (Sandalwood) Extract, Simmondsia Chinesis (Jojoba) Seed Oil, Tocopherol, Trehalose, Vanilla Planifolia Fruit Extract, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Super Power

Sunscreen

MOUSSE

Broad Spectrum SPF 50

Water resistant (80 minutes)

Supergoop!

7.1 fl. oz. / 200 mL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75936-504-112023-04-08C16284748780-1d6a99b39-b6ca-a426-e053-dadaa90af4c2Super Power Sunscreen Mousse SPF 50
75936-504-112022-01-28C16284748780-1d6a99b39-b6ca-a426-e053-dadaa90af4c2Super Power Sunscreen Mousse SPF 50

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-50475936-504-11

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 48 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
f8d8ed00-4cab-76eb-e053-6294a90af4da7d6f46cd-2a9c-4c66-9fa5-e84a2fcb99fb2023-04-08WarningsExact identifier
spl set id: 7d6f46cd-2a9c-4c66-9fa5-e84a2fcb99fb

Reported adverse events (FAERS/openFDA)#

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