UV Daily Deep Tint

Manufacturer
CP Skin Health Group, Inc. | Swiss-American CDMO, LLC
Effective date
2024-05-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:12:22

Label at a glance#

ProductUV Daily Deep Tint
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure9 sections

Indications and uses

Helps prevent sunburn. If used as directed with other sun protection measure (See Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Use a water-resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. 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 of 15 or higher and other sun protection measures including: limit time in the sun, especially fro...

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

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. Stop use and ask a physician if rash occurs. If product is swallowed get medical help or contact a Poison Control Center right away.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Uses

OTC - PURPOSE SECTION

Helps prevent sunburn. If used as directed with other sun protection measure (See Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn. If used as directed with other sun protection measure (See Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Use a water-resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. 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 of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 am to 2 pm. Wear long-sleeve shirts, pants, hats, and sunglasses. Children under 6 months: ask a physician.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate    7.5%

Zinc Oxide   9.0%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, petrolatum, isopropyl palmitate, dimethicone, cetearyl alcohol, oleth-3 phosphate, phenoxyethanol, octyldodecyl neopentanoate, ethylhexyl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, polyisobutene, cetearyl glucoside, polyether-1, butylene glycol, PEG-7 trimethylolpropane cocnut ether, sodium hyaluronate, citric acid, iodopropynyl butylcarbamate, tocopheryl acetate, triethoxycaprylylsilane, iorn oxides

Questions

OTC - QUESTIONS SECTION

Call toll free 1-800-633-8872

Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UV Daily Deep Tint UCUV Daily Deep Tint UC

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72043-2920-1UV Daily Deep Tint50 g in 1 BOTTLELOTION501
72043-2920-2UV Daily Deep Tint2 g in 1 PACKETLOTION21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72043-2920UV DAILY DEEP TINT (OCTINOXATE, ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.]1Current NDC, 2 package rows20240511_c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b450.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72043-292072043-2920-1, 72043-2920-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
UV Daily Deep TintOCTINOXATE, ZINC OXIDE SUNSCREENCP Skin Health Group, Inc.c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b4502024-05-09WarningsExact identifier
ndc (package): 72043-2920-1
ndc (package): 72043-2920-2
ndc (product): 72043-2920
ndc11 (package): 72043292002
ndc11 (package): 72043292001
spl id: 79386a40-776e-47d1-8909-88776673d1a9
spl set id: c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b450

Reported adverse events (FAERS/openFDA)#

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