FDA.reportPublic FDA data

Daily Doctor Hand Care Fragrance Free

Manufacturer
Soleo Cosmetic Co., Ltd.
Effective date
2020-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:37

Label at a glance#

ProductDaily Doctor Hand Care Fragrance Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Rub onto hands until absorbed.

Storage and handling

Store below 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.066%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • Hand sanitizer to decrease bacteria on the skin persistently. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of eye contact, flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Rub onto hands until absorbed.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Caprylic and Capric Triglyceride, Polysorbate 60, Isopropyl Myristate, Sorbitan Sesquioleate, Carbomer, Arginine, Phenoxyethanol, Disodium EDTA, Sodium Hyaluronate, Green tea Extract, Jojoba Oil, Almond Oil, Olive Oil, Camelia Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71693-00171693-001-01, 71693-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
JOJOBA OIL724GKU717MIACT
ALMOND OIL66YXD4DKO9IACT
AVOCADO OIL6VNO72PFC1IACT
OLIVE OIL6UYK2W1W1EIACT
CAMELLIA OILT1PE06G0VEIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
POLYSORBATE 60CAL22UVI4MIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ARGININE94ZLA3W45FIACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT

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
b3f67e96-39e0-d0a3-e053-2a95a90a7a9bb71dba13-f3f7-418f-96a3-bb6ee376eabb2020-11-12WarningsExact identifier
spl set id: b71dba13-f3f7-418f-96a3-bb6ee376eabb

Reported adverse events (FAERS/openFDA)#

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