Skintillate Hand Sanitizer

Manufacturer
D-Time Limited Liability Company
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:44:38

Label at a glance#

ProductSkintillate Hand Sanitizer
Active ingredientALCOHOL, ISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Adults and children over 2 years: For occasional and personal domestic use. Supervise children when they use this product. Spray onto hands and rub thoroughly for at least 30 seconds. Allow to dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol (80%)
Ethyl Alcohol (75%), Isopropyl Alcohol (5%)

​Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Use

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of bacteria.

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and consult a healthcare professional if irritation develops.

Flammable. Keep away from heat and flame.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years: For occasional and personal domestic use. Supervise children when they use this product. Spray onto hands and rub thoroughly for at least 30 seconds. Allow to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Hydrogen Peroxide , Glycerin, Hyaluronic Acid, Bergamot leaf oil, Lavender Flower Oil, Centella Asiatica Extract, Sodium pyruvate

Other information
Store at 68 0 to 70 0 F (20 0 to 25 0C). May discolor certain fabrics or surfaces.
Questions? 1-844-800-6858

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 1Label 1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75306-003-01Skintillate Hand Sanitizer30 mL in 1 BOTTLE, PLASTICSOLUTION302
75306-003-02Skintillate Hand Sanitizer50 mL in 1 BOTTLE, PLASTICSOLUTION502
75306-003-03Skintillate Hand Sanitizer60 mL in 1 BOTTLE, PLASTICSOLUTION602
75306-003-04Skintillate Hand Sanitizer100 mL in 1 BOTTLE, PLASTICSOLUTION1002
75306-003-05Skintillate Hand Sanitizer120 mL in 1 BOTTLE, PLASTICSOLUTION1202
75306-003-06Skintillate Hand Sanitizer160 mL in 1 BOTTLE, PLASTICSOLUTION1602
75306-003-07Skintillate Hand Sanitizer200 mL in 1 BOTTLE, PLASTICSOLUTION2002
75306-003-08Skintillate Hand Sanitizer250 mL in 1 BOTTLE, PLASTICSOLUTION2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75306-003SKINTILLATE HAND SANITIZER (ALCOHOL, ISOPROPYL ALCOHOL) SOLUTION [D-TIME LIMITED LIABILITY COMPANY]2Legacy NDC, 8 package rows20211103_0923fbdc-b85a-4113-a07f-715820fffa3f.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML · Source PDF

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
cfd125d2-54bc-a06a-e053-2a95a90aaf370923fbdc-b85a-4113-a07f-715820fffa3f2021-11-02WarningsExact identifier
spl id: cfd125d2-54bc-a06a-e053-2a95a90aaf37
spl set id: 0923fbdc-b85a-4113-a07f-715820fffa3f

Reported adverse events (FAERS/openFDA)#

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