CKP SAN-40 Gel

Manufacturer
CK Polymers
Effective date
2020-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:27

Label at a glance#

ProductCKP SAN-40 Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CKP SAN-40 Gel

NDC 78235-997-40

label-40label-40

MANUFACTURER:

United States

CK Polymers, LLC

4801 Woodway Drive

Suite 275E

Houston, TX 77056

EMERGENCY PHONE:

United States

CHEMTREC

1-800-424-9300 (24 hours)

BUSINESS PHONE:

United States

1-713-979-3970

LABELING AND CLASSIFICATIONS:

Classification of the substance or mixture according to Hazardous Communication Standard, 29 CFR 1910.1200:

Eye irritation, category 2A

Flammable liquids, category 2

Signal word: Danger

Hazard-determining components of labeling:

Ethanol

HAZARD STATEMENTS:

H224 Highly flammable liquid and vapor

H319 Causes serious eye irritation

PRECAUTIONARY STATEMENTS:

P210 Keep away from heat/sparks/open flames/hot surfaces. No smoking

P233 Keep container tightly closed

P240 Ground/bond container and receiving equipment

P241 Use explosion-proof electrical/ventilating/lighting/equipment

P242 Use only non-sparking tools

P243 Take precautionary measures against static discharge

P264 Wash hands thoroughly after handling

P280 Wear protective gloves/protective clothing/eye protection/face protection

P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower.

P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing

P337+P313 If eye irritation persists: Get medical advice/attention

P370+P378 In case of fire: Use agents recommended in section 5 to extinguish

P403+P235 Store in a well-ventilated place. Keep cool

P501 Dispose of contents/container in accordance with local regulations.

TRANSPORTATION:

UN Number: 1170

Proper shipping name: Ethanol Solution

Packing group: II

Hazard class: 3

California Proposition 65: None of the ingredients are listed.

Refer to the SDS for full guidelines and product information

NDC 78235-997-50

label-50label-50

NDC 78235-997-60

label-60label-60

NDC 78235-997-70

label-70label-70

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78235-997-40CKP SAN-40 Gel1249.19 L in 1 BOTTLEGEL1249.191
78235-997-50CKP SAN-40 Gel3.78541 L in 1 BOTTLEGEL3.785411
78235-997-60CKP SAN-40 Gel18.9271 L in 1 BOTTLEGEL18.92711
78235-997-70CKP SAN-40 Gel208.198 L in 1 BOTTLEGEL208.1981

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78235-997CKP SAN-40 GEL (HAND SANITIZER) GEL [CK POLYMERS]1Legacy NDC, 4 package rows20200630_20267a91-7333-4eef-8d3b-3bbb8db74bdf.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78235-99778235-997-40, 78235-997-50, 78235-997-60, 78235-997-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
fb03f481-014b-40a9-b442-6c4ae01d61d620267a91-7333-4eef-8d3b-3bbb8db74bdf2020-06-25Exact identifier
spl id: fb03f481-014b-40a9-b442-6c4ae01d61d6
spl set id: 20267a91-7333-4eef-8d3b-3bbb8db74bdf

Reported adverse events (FAERS/openFDA)#

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