Hand sanitizer lotion

Manufacturer
McKesson Medical-Surgical | Central Solutions
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:38:37

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Ethanol 70%

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • An effective antimicrobial hand cleanser for topical application
  • Recommended for repeated use
  • Reduces transient microorganisms on intact skin
  • Keeps hands from drying out due to repeated uses

WARNINGS SECTION

Warnings

  • For External Use Only
  • Flammable, keep away from fire or open flame

OTC - STOP USE SECTION

When using this product:

  • Avoid contact with eyes
  • In case of eye contact, flush with water for 15 minutes
  • Discontinue use and see a doctor if irritation occurs
  • Avoid contact with broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wet hands thoroughly with product. Allow to dry without wiping. Use no water or

towels

OTHER SAFETY INFORMATION

Other information

  • Not tested on animals

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butylene
Glycol, Calcium Pantothenate (Vitamin B5), Cetyl Alcohol, Fragrance, Glycerin, Glyceryl
Laurate, Hydroxypropyl Cellulose, Isopropyl Myristate, Maltodextrin, Niacinamide
(Vitamin B3), Pyridoxine HCl (Vitamin B6), Silica, Sodium Ascorbyl Phosphate (Vitamin
C),Sodium Starch Octenylsuccinate, Titanium Dioxide, Tocopherol (Vitamin E),
Tocopheryl Acetate (Vitamin E), Trehalose, Water

OTC - QUESTIONS SECTION

Questions?
Call 1-800-777-4908

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

68599-5207-1

Hand Sanitizer Lotion

An antiseptic hand sanitizer with moisturizers and
emollients to help prevent drying of the skin.

NET CONTENTS 8 fl oz (237 mL)

MFR # 53-LHS8

eacheach

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1809903ethanol 70 % Topical LotionPSN2
1809903ethanol 0.7 ML/ML Topical LotionSCD2
1809903ethanol 70 % Topical LotionSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68599-5207-1Hand Sanitizer237 mL in 1 BOTTLELOTION2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68599-5207HAND SANITIZER (LOTIONIZED HAND SANITIZER) LOTION [MCKESSON MEDICAL-SURGICAL]2Current NDC, 1 package rows20241123_2253f369-ae8a-0432-e063-6294a90aee84.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68599-520768599-5207-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
Hand SanitizerLOTIONIZED HAND SANITIZERMcKesson Medical-Surgical2253f369-ae8a-0432-e063-6294a90aee842024-11-21WarningsExact identifier
ndc (package): 68599-5207-1
ndc (product): 68599-5207
ndc11 (package): 68599520701
spl id: 2772436f-4118-c6d8-e063-6394a90ab826
spl set id: 2253f369-ae8a-0432-e063-6294a90aee84

Reported adverse events (FAERS/openFDA)#

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