Hand Sanitizer

Manufacturer
Hidden Springs Manufacturing LLC. | HIDDEN SPRINGS MFG., CO. LLC
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:37

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% 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. 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

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 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.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, propylene glycol, squalane, fragrance, aloe barbadensis leaf juice, tocopheryl acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

010 mL NDC: 78614-435-10

10mL label10mL label

030 mL NDC: 78614-435-30

30 mL label30 mL label

050 mL NDC: 78614-435-50

050 mL NDC: 78614-435-50050 mL NDC: 78614-435-50

050 mL NDC: 78614-435-50050 mL NDC: 78614-435-50

118 mL NDC: 78614-435-04

118 mL NDC: 78614-435-04118 mL NDC: 78614-435-04

473 mL NDC: 78614-435-16

473 mL label473 mL label

473 mL NDC: 78614-435-16473 mL NDC: 78614-435-16

1892 mL NDC: 78614-435-64

1892 mL NDC: 78614-435-641892 mL NDC: 78614-435-64

236 mL NDC: 78614-435-08

8oz label8oz label

236 mL NDC: 78614-435-08236 mL NDC: 78614-435-08

3785 mL NDC: 78614-435-28

3785 mL NDC: 78614-435-283785 mL NDC: 78614-435-28

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78614-435-04Hand Sanitizer118 mL in 1 BOTTLE, PLASTICGEL1181
78614-435-08Hand Sanitizer236.59 mL in 1 BOTTLE, PUMPGEL236.591
78614-435-10Hand Sanitizer10 mL in 1 BOTTLE, SPRAYGEL101
78614-435-16Hand Sanitizer473 mL in 1 BOTTLE, PLASTICGEL4731
78614-435-28Hand Sanitizer3785.41 mL in 1 BOTTLE, PLASTICGEL3785.411
78614-435-30Hand Sanitizer30 mL in 1 TUBEGEL301
78614-435-50Hand Sanitizer50 mL in 1 BOTTLE, PLASTICGEL501
78614-435-64Hand Sanitizer1892.71 mL in 1 BOTTLE, PUMPGEL1892.711

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78614-435HAND SANITIZER (ALCOHOL) GEL [HIDDEN SPRINGS MANUFACTURING LLC.]1Legacy NDC, 8 package rows20200709_a706164d-fa79-82a4-e053-2a95a90a06ae.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a706164d-fa68-82a4-e053-2a95a90a06aea706164d-fa79-82a4-e053-2a95a90a06ae2020-06-01WarningsExact identifier
spl id: a706164d-fa68-82a4-e053-2a95a90a06ae
spl set id: a706164d-fa79-82a4-e053-2a95a90a06ae

Reported adverse events (FAERS/openFDA)#

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