FDA.reportPublic FDA data

Safeguard Moisturizing Hand Sanitizer Ocean Breeze

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2023-05-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:31:14

Label at a glance#

ProductSafeguard Moisturizing Hand Sanitizer Ocean Breeze
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

For Handwashing to decrease bacteria on skin Recommended for repeated use

Dosage and administration

Dispense a small amount of liquid into palm of hand. Rub thoroughly over all surfaces of both hands Rub hands together until dry. Do not rinse.

Storage and handling

Store in a cool dry place below 104ºF. Seal bottle completely after use.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 69.9% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For Handwashing to decrease bacteria on skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flame

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with eyes,in case of contact, rinse with water immediately.
  • If irritation develops, discontinue use and consult a doctor.

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 except under adult supervision. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Dispense a small amount of liquid into palm of hand.
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together until dry. Do not rinse.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place below 104ºF. Seal bottle completely after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, isopropyl alcohol,butylene glycol, fragrance, carbomer, aminomethyl propanol, isopropyl myristate, tocopheryl acetate, blue 1, red 33

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Safeguard TM

MOISTURIZING

HAND SANITIZER

69.9% Alcohol Hand Sanitizer

Ocean

Breeze

12 FL OZ (355 mL)

SafeguardSafeguard

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69423-546-352023-05-18C16284748780-1c7ccaba7-1ca7-fd44-e053-dadaa90aa01bbcbd8180-157b-e055-e053-2995a90a0f1d
69423-546-352023-01-30C16284748780-1c7ccaba7-1ca7-fd44-e053-dadaa90aa01bbcbd8180-157b-e055-e053-2995a90a0f1d
69423-546-352021-11-14C16284748780-1c7ccaba7-1ca7-fd44-e053-dadaa90aa01bbcbd8180-157b-e055-e053-2995a90a0f1d
69423-546-352021-07-23C16284748780-1c7ccaba7-1ca7-fd44-e053-dadaa90aa01bbcbd8180-157b-e055-e053-2995a90a0f1d

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-54669423-546-35

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
D&C RED NO. 339DBA0SBB0LIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
fbfa23c2-dadf-4f45-e053-6394a90a4fefbcbd8180-157b-e055-e053-2995a90a0f1d2023-05-18WarningsExact identifier
spl id: fbfa23c2-dadf-4f45-e053-6394a90a4fef
spl set id: bcbd8180-157b-e055-e053-2995a90a0f1d

Reported adverse events (FAERS/openFDA)#

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