FDA.reportPublic FDA data

Everlit Survival Antiseptic Wipe

Manufacturer
EVERLIT GLOBAL INC. | Changzhou Maokang Medical Products Co., Ltd
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:34:34

Label at a glance#

ProductEverlit Survival Antiseptic Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Sanitize Hands/ Clean Wounds

Dosage and administration

Tear open packet, unfold towelett, use to cleanse desired skin area. Discard towelette appropriately after use. Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

To disinfect skin surfaces

Uses

INDICATIONS & USAGE SECTION

Sanitize Hands/ Clean Wounds

Warnings

WARNINGS SECTION

Avoid contact with eyes, if happens, rinse thoroughly with water

For External Use Only

If pain, irritation, swelling, or infection develops, discontinue use and consult a phsicien

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental swallowing, seek medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, unfold towelett, use to cleanse desired skin area. Discard towelette appropriately after use.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sodium Bicaronate

Directions

RECENT MAJOR CHANGES SECTION

Tear open packet, unfold towelett, use to cleanse desired skin area. Discard towelette appropriately after use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NANA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN2
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD2
1038558benzalkonium chloride 0.13 % Topical ClothSY2
1038558benzalkonium chloride 0.13 % Topical SwabSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY2
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83807-024-01Everlit Survival Antiseptic Wipe1 in 1 PACKETCLOTH12

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83807-02483807-024-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOIACT
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
Everlit Survival Antiseptic WipeANTISEPTIC WIPEEVERLIT GLOBAL INC.3a03f7e6-cc74-22a2-e063-6394a90a5f9f2026-01-23WarningsExact identifier
ndc (package): 83807-024-01
ndc (product): 83807-024
ndc11 (package): 83807002401
spl id: 49131f87-b57a-8036-e063-6294a90ae490
spl set id: 3a03f7e6-cc74-22a2-e063-6394a90a5f9f

Reported adverse events (FAERS/openFDA)#

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