Naked One and Done Cream Light

Manufacturer
Autumn Harp Inc.
Effective date
2019-09-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:09:33

Label at a glance#

ProductNaked One and Done Cream Light
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure7 sections

Dosage and administration

For sunscreen use: Apply liberally 15 minutes before sun exposer. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Sun Protection Measures. Spending time in the 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...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.5%

Zinc Oxide 3.4%

WARNINGS: For external use only.

WARNINGS SECTION

Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs.

DIRECTIONS:

OTC - WHEN USING SECTION

For sunscreen use: Apply liberally 15 minutes before sun exposer. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Sun Protection Measures. Spending time in the 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. Children under 6 months of age: Ask a doctor.

Other Information:

OTHER SAFETY INFORMATION

​Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isododecane, Cyclopentasiloxane, Adipic Acid / Neopentyl Glycol Crosspolymer, Lauryl Dimethicone, Aloe Barbadensis Leaf Juice, Titanium Dioxide, Polyglyceryl-6 Polyricinoleate, Dimethicone/Vinyl Dimethicone Crosspolymer, Propylene Glycol, Isononyl Isononanoate, Hydrogenated Polyisobutene, Polyglyceryl-2 Isostearate, Glycerin, Phenoxyethanol, Propanediol, Dimethicone Crosspolymer, Disteardimonium Hectorite, Isopropyl Myristate, Iron Oxide (CI 77492), Sodium Chloride, Glycyrrhiza Glabra (Licorice) Root Extract, Aspergillus Ferment, Xanthan Gum, Isoceteth-10, Silica, Iron Oxides (CI 77491), Isopropyl Titanium Triisostearate, Triethoxycaprylylsilane, Stearalkonium Hectorite, Evodia Rutaecarpa Fruit Extract, Ethoxydiglycol, Cyclotetrasiloxane, Dimethylcyclosiloxane, Iron Oxides (CI 77499), Propylene Carbonate, Polyhydroxystearic Acid, BHT, Sorbic Acid, may contain: titanium dioxide, iron oxides

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-784-URBAN(8722)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51514-0343-12021-01-29C16284748780-1ba0f9c33-28cc-a910-e053-dadaa90a0b85Naked Skin One and Done, Light

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51514-034351514-0343-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 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
93798e61-6da4-b8db-e053-2a95a90a806831f614e2-9298-0c47-e054-00144ff8d46c2019-09-26WarningsExact identifier
spl id: 93798e61-6da4-b8db-e053-2a95a90a8068
spl set id: 31f614e2-9298-0c47-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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