FDA.reportPublic FDA data

Sanitizer gel

Manufacturer
Pop Fizz Designs
Effective date
2022-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:51:36

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

Drug facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand sanitizer box drug facts labelHand sanitizer box drug facts labelDrug facts labelDrug facts label

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame. Stop use and ask doctor if irritation or rash appears.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump as needed into the palm of hands. Rub hands together quickly until dry. Children under 6 years old should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

Store below 118°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbendensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethonoamine, Fragrance, FD&C Blue No. 1, D&C Red No. 33.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73884-001-112024-01-30C16284748780-11030e365-4595-111a-e063-dadaa90a10e2Sanitizer gel
73884-002-122024-01-30C16284748780-11030e365-4595-111a-e063-dadaa90a10e2Sanitizer gel
73884-002-132024-01-30C16284748780-11030e365-4595-111a-e063-dadaa90a10e2Sanitizer gel
73884-002-142024-01-30C16284748780-11030e365-4595-111a-e063-dadaa90a10e2Sanitizer gel
73884-002-232024-01-30C16284748780-11030e365-4595-111a-e063-dadaa90a10e2Sanitizer gel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73884-00273884-002-02, 73884-002-12, 73884-002-03, 73884-002-13, 73884-002-04, 73884-002-14, 73884-002-05, 73884-002-23
73884-00173884-001-01, 73884-001-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
MALTODEXTRIN7CVR7L4A2DIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
MALTODEXTRIN7CVR7L4A2DIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

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
a1629152-276f-8040-e053-2a95a90a25daa1629152-276e-8040-e053-2a95a90a25da2022-10-01WarningsExact identifier
spl id: a1629152-276f-8040-e053-2a95a90a25da
spl set id: a1629152-276e-8040-e053-2a95a90a25da

Reported adverse events (FAERS/openFDA)#

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