FDA.reportPublic FDA data

Moisturising Hand Sanitizer

Manufacturer
RESCUE SPA, INC. | Oceanic SA
Effective date
2022-03-29
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:48:58

Label at a glance#

ProductMoisturising Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store at the temperature below 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help reduce bacteria that potentially can cause disease.
  • Recommended for repeated, frequent use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

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.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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

  • Place enough product in your palm to thoroughly cover your hands.
  • Rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store at the temperature below 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water USP, acrylates/c10-30 alkyl acrylates crosspolymer, glycerin, hyaluronic acid, triethanolamine, phenoxyethanol, ethylhexylglycerin, fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

bottle 250mL 250250

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

tube 70mL 70mL70mL

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

Sachet 50 x 0.07 fl. oz. (50 x 2 mL)

outer labelouter labelinner labelinner label

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

1.69 fl.oz. / 50 mL

Outer labelOuter labelInner labelInner label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2282911ethanol 71 % Topical GelPSN8
2282911ethanol 0.71 ML/ML Topical GelSCD8
2282911ethanol 71 % Topical GelSY8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79535-7001-02023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer
79535-7001-12023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer
79535-7001-22023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer
79535-7001-32023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer
79535-7001-42023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer
79535-7001-52023-07-28C16284748780-10191ceaa-6b81-198a-e063-dbdaa90aec3eRescue Me Moisturizing Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79535-7001-0Moisturising Hand Sanitizer2 mL in 1 POUCHGEL28
79535-7001-1Moisturising Hand Sanitizer1 in 1 CARTONGEL18
79535-7001-1Moisturising Hand Sanitizer50 in 1 POUCHGEL508
79535-7001-2Moisturising Hand Sanitizer1 in 1 CARTONGEL18
79535-7001-2Moisturising Hand Sanitizer50 mL in 1 TUBEGEL508
79535-7001-3Moisturising Hand Sanitizer50 in 1 CARTONGEL508
79535-7001-3Moisturising Hand Sanitizer2 mL in 1 POUCHGEL28
79535-7001-4Moisturising Hand Sanitizer250 mL in 1 BOTTLEGEL2508
79535-7001-4Moisturising Hand Sanitizer1 in 1 CARTONGEL18
79535-7001-5Moisturising Hand Sanitizer70 mL in 1 TUBEGEL708
79535-7001-5Moisturising Hand Sanitizer1 in 1 CARTONGEL18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79535-7001MOISTURISING HAND SANITIZER (ALCOHOL) GEL [RESCUE SPA, INC.]8Legacy NDC, 11 package rows20220330_ab043951-36de-6cc9-e053-2a95a90ac80c.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79535-700179535-7001-1, 79535-7001-0, 79535-7001-2, 79535-7001-3, 79535-7001-5, 79535-7001-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT

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
db5d42ba-9b8a-765c-e053-2995a90af1c9ab043951-36de-6cc9-e053-2a95a90ac80c2022-03-29WarningsExact identifier
spl id: db5d42ba-9b8a-765c-e053-2995a90af1c9
spl set id: ab043951-36de-6cc9-e053-2a95a90ac80c

Reported adverse events (FAERS/openFDA)#

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