NARS LAGUNA BODY TINT

Manufacturer
NARS Cosmetics
Effective date
2018-11-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:45:10

Label at a glance#

ProductNARS LAGUNA BODY TINT
Active ingredientAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE
Label structure10 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

For sunscreen use: 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...

Storage and handling

protect this product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%
Homosalate 10%
Octinoxate 7.4%
Octocrylene 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • 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 a.m. - 2 p.m.
    • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water ∙ Glycerin ∙ Propanediol ∙ Butylene Glycol ∙ Decyl Isostearate ∙ Cocos Nucifera (Coconut) Oil ∙ Gardenia Taitensis Flower Extract ∙ Curcuma Longa (Turmeric) Root Extract ∙ Calophyllum Inophyllum Seed Oil ∙ Vanilla Tahitensis Fruit Extract ∙ Isostearyl Isostearate ∙ Acrylates/Beheneth-25 Methacrylate Copolymer ∙ PPG-8-Ceteth-20 ∙ Sorbeth-30 Tetraisostearate ∙ Sorbitan Sesquiisostearate ∙ Polyurethane-35 ∙ Dipropylene Glycol ∙ BHT ∙ Potassium Hydroxide ∙ Trisodium EDTA ∙ Fragrance ∙ Phenoxyethanol ∙ Mica ∙ Titanium Dioxide ∙ Iron Oxides ∙

Other information

STORAGE AND HANDLING SECTION

  • protect this product in this container from excessive heat and direct sun

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-888-788-NARS

PRINCIPAL DISPLAY PANEL - 100 mL Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NARS

LAGUNA BODY TINT
BROAD SPECTRUM
SPF 30 SUNSCREEN

NET WT. 3.8 Oz. 100 mL

PRINCIPAL DISPLAY PANEL - 100 mL Tube Carton
PRINCIPAL DISPLAY PANEL - 100 mL Tube Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13734-159-602023-09-11C16284748780-1f386c64a-3ac4-0266-e053-dadaa90a7c1aNARS LAGUNA BODY TINT
13734-159-602023-01-30C16284748780-1f386c64a-3ac4-0266-e053-dadaa90a7c1aNARS LAGUNA BODY TINT

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13734-15913734-159-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
39a742be-5938-4a88-8ffb-f7f9577ffa056dd7d83f-f916-47d3-8033-1b725ea0e8a82023-09-11WarningsExact identifier
spl set id: 6dd7d83f-f916-47d3-8033-1b725ea0e8a8

Reported adverse events (FAERS/openFDA)#

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