FDA.reportPublic FDA data

DG Baby

Manufacturer
Dolgencorp Inc.
Effective date
2019-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:48

Label at a glance#

ProductDG Baby FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

■ wet hands thoroughly with product and allow to dry without wiping ■ for children under 6, use only under adult supervision ■ not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only, hands only

When using this product

OTC - WHEN USING SECTION

■ avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water ■ avoid contact with broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or redness develops ■ condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands thoroughly with product and allow to dry without wiping ■ for children under 6, use only under adult supervision ■ not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

cetrimonium chloride, citrus reticulata X C. sinensis peel extract, disodium cocoamphodiacetate, PEG-12 dimethicone, tocopheryl acetate, water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55910-989-802021-07-23C16284748780-1c7ccaba7-1617-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-989DG BABY FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DOLGENCORP INC.]1Legacy NDC20190417_86ad36a5-08b7-7792-e053-2a91aa0a2f6b.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55910-98955910-989-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-12 DIMETHICONEZEL54N6W95IACT
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
86ad176c-013d-144f-e053-2a91aa0a986d86ad36a5-08b7-7792-e053-2a91aa0a2f6b2019-04-16WarningsExact identifier
spl id: 86ad176c-013d-144f-e053-2a91aa0a986d
spl set id: 86ad36a5-08b7-7792-e053-2a91aa0a2f6b

Reported adverse events (FAERS/openFDA)#

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