FDA.reportPublic FDA data

Rejuviel

Manufacturer
Private Label Productions, LLC
Effective date
2023-09-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:26:27

Label at a glance#

ProductRejuviel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer helps decrease bacteria on skin when soap, water, towel are not available. Recommended for repeated use.

Dosage and administration

Apply as needed onto the palms and throughly spread on both hands together briskly until dry. Children under 6 years of age should be supervised when using.

Storage and handling

Store at 20' C (68'F - 77'F). May discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

70% Ethanol (SD Alcohol)

Purpose

OTC - PURPOSE SECTION

Anti-Septic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer helps decrease bacteria on skin when soap, water, towel are not available. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product, do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts for longer than 72 hours.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed onto the palms and throughly spread on both hands together briskly until dry. Children under 6 years of age should be supervised when using.

Other Information

STORAGE AND HANDLING SECTION

Store at 20' C (68'F - 77'F). May discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), 1,3-Propanediol, PEG600 (PEG-12), Glycerin, Carbomer, Triethanaolamine

HOW SUPPLIED SECTION

Manufactured by / Fabrique par: Private Label Productions LLC, Bonita Springs, FL 34135

With / Avec:

Rejuviel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77632-070-992023-09-07C16284748780-1d6a99b39-756b-a426-e053-dadaa90af4c2a1c7b0b8-c131-9926-e053-2a95a90a0534
77632-070-992022-01-28C16284748780-1d6a99b39-756b-a426-e053-dadaa90af4c2a1c7b0b8-c131-9926-e053-2a95a90a0534

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77632-07077632-070-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
POLYETHYLENE GLYCOL 600NL4J9F21N9IACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
PROPANEDIOL5965N8W85TIACT

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
04bf4c41-dea1-2873-e063-6394a90a9618a1c7b0b8-c131-9926-e053-2a95a90a05342023-09-07WarningsExact identifier
spl id: 04bf4c41-dea1-2873-e063-6394a90a9618
spl set id: a1c7b0b8-c131-9926-e053-2a95a90a0534

Reported adverse events (FAERS/openFDA)#

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