AutoSpritz

Manufacturer
ORIGYN LLC | Guangzhou Shiruoni Cosmetics Co. Ltd
Effective date
2020-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:35

Label at a glance#

ProductAutoSpritz
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Glycerin, hydrogen peroxide, purified water USP

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

KEEP OUT OF REACH OF CHILDREN

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.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are not available

WARNINGS

WARNINGS SECTION

  • For external use only. Flammable. Keep away from heat or flame.
  • Do not use
    • for children less than 2 months of age
    • on open skin wounds
  • When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
  • Stop use and ask a doctor if irritation of rash occurs. These may be signs of a serious health condition.
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Refill Bottle 33.8 fl oz (1L)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Refill Bottle 33.8 fl oz (1L)Refill Bottle 33.8 fl oz (1L)

Auto Dispenser Bottle 12 fl oz (355ml)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Auto Dispenser Bottle 12 fl oz (355ml)Auto Dispenser Bottle 12 fl oz (355ml)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79281-010-012022-01-28C16284748780-1d6a99b39-42ae-a426-e053-dadaa90af4c27a5b3a50-5d30-4fe1-b9f5-8492228b5987
79281-010-022022-01-28C16284748780-1d6a99b39-42ae-a426-e053-dadaa90af4c27a5b3a50-5d30-4fe1-b9f5-8492228b5987

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79281-010-01AutoSpritz1 L in 1 BOTTLESOLUTION11
79281-010-02AutoSpritz0.355 L in 1 BOTTLE, DISPENSINGSOLUTION0.3551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79281-010AUTOSPRITZ (ALCOHOL) SOLUTION [ORIGYN LLC]1Legacy NDC, 2 package rows20200709_7a5b3a50-5d30-4fe1-b9f5-8492228b5987.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79281-01079281-010-01, 79281-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
7639f49a-73ea-4117-97fa-1fa45ee1e2737a5b3a50-5d30-4fe1-b9f5-8492228b59872020-07-01WarningsExact identifier
spl id: 7639f49a-73ea-4117-97fa-1fa45ee1e273
spl set id: 7a5b3a50-5d30-4fe1-b9f5-8492228b5987

Reported adverse events (FAERS/openFDA)#

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