FDA.reportPublic FDA data

Invisi Shield Anti Bacterial

Manufacturer
Creative Essences Inc
Effective date
2022-12-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:42:37

Label at a glance#

ProductInvisi Shield Anti Bacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Kills germs and bacteria a person will come in contact with.

Label contents#

Full prescribing information#

Invisi Shield Label Warning

WARNINGS SECTION

Label Warning StatementLabel Warning StatementNDC 70658-118-29NDC 70658-118-29NDC#70658-118-29NDC#70658-118-29NDC#70658-118-29NDC#70658-118-29Package Label NDC #70658-118-29Package Label NDC #70658-118-29

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, propylene glycol, octyl palmitate, stearic acid, glyceryl stearate, castor oil, dimethicone, disodium edta, mineral oil, simmondsia chinensis (jojoba) oil, aloe babradensis leaf juice, trietholamine, 2-bromo-2-nitro-1,3-propanediol, fragrance

Uses

INDICATIONS & USAGE SECTION

Kills germs and bacteria a person will come in contact with.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children 5 and under use with adult supervision. In case of accidental ingestion, get medical help or contact Poison Control Center immediately.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Invisi Shield Long Lasting Anti Bacterial Lotion NDC#70658-118-29

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC #70658-118-29NDC #70658-118-29

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70658-118-292024-01-30C16284748780-1d6a99b3a-01c9-a426-e053-dadaa90af4c2Invisi-Shield
70658-118-292022-06-09C16284748780-1d6a99b3a-01c9-a426-e053-dadaa90af4c2Invisi-Shield
70658-118-292022-01-28C16284748780-1d6a99b3a-01c9-a426-e053-dadaa90af4c2Invisi-Shield

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70658-11870658-118-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
ETHYLHEXYL PALMITATE2865993309IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
LIGHT MINERAL OILN6K5787QVPIACT
BRONOPOL6PU1E16C9WIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
CASTOR OILD5340Y2I9GIACT
JOJOBA OIL724GKU717MIACT
STEARIC ACID4ELV7Z65APIACT

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
f0c0aebf-485c-cc35-e053-2995a90a9f1ea25407d8-f857-b4bb-e053-2995a90a4db52022-12-26WarningsExact identifier
spl id: f0c0aebf-485c-cc35-e053-2995a90a9f1e
spl set id: a25407d8-f857-b4bb-e053-2995a90a4db5

Reported adverse events (FAERS/openFDA)#

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