FDA.reportPublic FDA data

Foam Hand Sanitizer

Manufacturer
Guangdong Kemei Pharmaceutical Technology Co., Ltd.
Effective date
2020-09-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:47

Label at a glance#

ProductFoam Hand Sanitizer
Active ingredientSODIUM CHLORIDE
Label structure12 sections

Indications and uses

Apply proper amount to palm, massage gently until foamy, then rinse with water.

Dosage and administration

Scope of application: Household and personal cleaning. Main Effect Effective inhibition of microorganisms category intestinal bacteria, pyogenic coccus.

Storage and handling

Keep tightly closed. Store between 32°F and 109°F

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Sodium chloride 1.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Apply proper amount to palm, massage gently until foamy, then rinse with water.

Warnings

WARNINGS SECTION

This product is for external use only.

When using this product In case of contact with eyes, rinse immediately with plenty of water.

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

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

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

When using this product In case of contact with eyes, rinse immediately with plenty of water.

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

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

OTC - STOP USE SECTION

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Scope of application: Household and personal cleaning.
Main Effect Effective inhibition of microorganisms category intestinal bacteria, pyogenic coccus.

Other information

STORAGE AND HANDLING SECTION

Keep tightly closed. Store between 32°F and 109°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citric acid, Cocoamidopropyl betaine, Coconut oil amide DEA, Disodium EDTA, DMDM hydantoin, Essence, Sodium lauryl alcohol polyether sulfate, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75132-013-01 236ml75132-013-01 236ml75132-013-02 300ml75132-013-02 300ml75132-013-06 3785mL75132-013-06 3785mL75132-013-04 500ml75132-013-04 500ml75132-013-05 1000ml75132-013-05 1000ml75132-013-03 450ml75132-013-03 450ml75132-013-07 5000mL75132-013-07 5000mL

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75132-013-012022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-022022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-032022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-042022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-052022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-062022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer
75132-013-072022-01-28C16284748780-1d6a99b39-7bfc-a426-e053-dadaa90af4c275132-013 Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75132-013-01Foam Hand Sanitizer236 mL in 1 BOTTLELIQUID2361
75132-013-02Foam Hand Sanitizer300 mL in 1 BOTTLELIQUID3001
75132-013-03Foam Hand Sanitizer450 mL in 1 BOTTLELIQUID4501
75132-013-04Foam Hand Sanitizer500 mL in 1 BOTTLELIQUID5001
75132-013-05Foam Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001
75132-013-06Foam Hand Sanitizer3785 mL in 1 BOTTLELIQUID37851
75132-013-07Foam Hand Sanitizer5000 mL in 1 BOTTLELIQUID50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75132-013FOAM HAND SANITIZER LIQUID [GUANGDONG KEMEI PHARMACEUTICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 7 package rows20200920_afa783c4-405d-cd70-e053-2a95a90ac94c.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75132-01375132-013-03, 75132-013-01, 75132-013-02, 75132-013-04, 75132-013-07, 75132-013-05, 75132-013-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO DIETHANOLAMIDE92005F972DIACT
SODIUM CHLORIDE451W47IQ8XACTIB
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
DMDM HYDANTOINBYR0546TOWIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
METHYL BENZOATE6618K1VJ9TIACT

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
afa78045-94dc-0360-e053-2995a90a6ccaafa783c4-405d-cd70-e053-2a95a90ac94c2020-09-19WarningsExact identifier
spl id: afa78045-94dc-0360-e053-2995a90a6cca
spl set id: afa783c4-405d-cd70-e053-2a95a90ac94c

Reported adverse events (FAERS/openFDA)#

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