FDA.reportPublic FDA data

Careone Spring Showers

Manufacturer
Spa Dent Inc | Apollo Health and Beauty Care
Effective date
2021-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:54

Label at a glance#

ProductCareone Spring Showers
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Helps eliminate bacteria on hands.

Dosage and administration

apply onto wet hands Lather and rinse thoroughly.

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient.

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on hands.

Warnings

WARNINGS SECTION

For external use only 

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of contact, rinse thoroughly with water. 

Stop use and ask a doctor.

OTC - STOP USE SECTION

If irritation or redness develops and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply onto wet hands
  • Lather and rinse thoroughly.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cetrimonium Chloride, Lauramidopropylamine Oxide, Glycerin, Lauamine Oxide, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Benzoate, Blue 1 (Cl 42090), Red 33 (Cl 17200).

PDP03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP03PDP03

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79147-01979147-019-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCO MONOETHANOLAMIDEC80684146DIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM BENZOATEOJ245FE5EUIACT
BASIC BLUE 192N74OA24DIACT
D&C RED NO. 339DBA0SBB0LIACT

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
ffb2af85-27f7-4ae4-a53c-6e8250f6b512eb06c239-1817-475d-8b0d-b59889b3176b2021-07-22WarningsExact identifier
spl id: ffb2af85-27f7-4ae4-a53c-6e8250f6b512
spl set id: eb06c239-1817-475d-8b0d-b59889b3176b

Reported adverse events (FAERS/openFDA)#

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