Sierra Soft Alcohol Hand Sanitizer

Manufacturer
CWGC LA Inc.
Effective date
2023-09-21
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 00:04:12

Label at a glance#

ProductSierra Soft Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

For sanitizing to reduce bacteria on the skin.

Dosage and administration

Apply one shot of foaming sanitizer to dry hands Rub into skin No rinsing required

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70 %

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For sanitizing to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Flammable :Keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. In case of eye contact, flush with water

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply one shot of foaming sanitizer to dry hands
  • Rub into skin
  • No rinsing required

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, BIS-PEG-12 Dimethicone, Propylene Glycol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN10
616805ethanol 0.7 ML/ML Topical FoamSCD10
616805ethanol 70 % Topical FoamSY10

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70415-002-01Sierra Soft Alcohol Hand Sanitizer1 L in 1 BOTTLELIQUID110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70415-002SIERRA SOFT ALCOHOL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [CWGC LA INC.]10Legacy NDC, 1 package rows20231214_3ba59fe1-387b-4915-bf43-23eab5a18a65.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
70415-00270415-002-01

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
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

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
05df821f-093e-180c-e063-6394a90ab4e03ba59fe1-387b-4915-bf43-23eab5a18a652023-09-21WarningsExact identifier
spl id: 05df821f-093e-180c-e063-6394a90ab4e0
spl set id: 3ba59fe1-387b-4915-bf43-23eab5a18a65

Reported adverse events (FAERS/openFDA)#

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