Trstay Face Self-Tanning Drops

Manufacturer
Yiwu Luoxin E Commerce Co Ltd
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:37:57

Label at a glance#

ProductTrstay Face Self-Tanning Drops
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

wart remover

INDICATIONS & USAGE SECTION

Apply twice daly(moring and night as a man and once as a woman.Afer apicaion, proeed with an acive masage for 3-5 minutes unthe product is fuy absorbed

WARNINGS SECTION

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier Keep out ofreach oi chidrenifvou ale preanant.nursing. otiaveanyunderving medca condion.consutyou healthcare provider before using the product

DOSAGE & ADMINISTRATION SECTION

For external use only.

OTC - DO NOT USE SECTION

Discontinue use if any irritation or adverse reaction occurs

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. lf contact occurs, rinse thoroughly with waterDiscontinue use if any irritation or adverse reaction occurs.

INACTIVE INGREDIENT SECTION

Acrylates copolymer, Ethyl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84756-358-01Trstay Face Self-Tanning Drops5 mL in 1 BOTTLELIQUID51
84756-358-02Trstay Face Self-Tanning Drops15 mL in 1 BOTTLELIQUID151
84756-358-03Trstay Face Self-Tanning Drops30 mL in 1 BOTTLELIQUID301
84756-358-04Trstay Face Self-Tanning Drops50 mL in 1 BOTTLELIQUID501
84756-358-05Trstay Face Self-Tanning Drops100 mL in 1 BOTTLELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84756-358TRSTAY FACE SELF-TANNING DROPS LIQUID [YIWU LUOXIN E COMMERCE CO LTD]15 package rows20241121_2741b37a-fd81-5963-e063-6294a90a6dda.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84756-35884756-358-01, 84756-358-02, 84756-358-03, 84756-358-04, 84756-358-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
2741b37a-fd82-5963-e063-6294a90a6dda2741b37a-fd81-5963-e063-6294a90a6dda2024-11-19WarningsExact identifier
spl id: 2741b37a-fd82-5963-e063-6294a90a6dda
spl set id: 2741b37a-fd81-5963-e063-6294a90a6dda

Reported adverse events (FAERS/openFDA)#

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