FDA.reportPublic FDA data

Geri Protect

Manufacturer
Geritrex LLC
Effective date
2015-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:32

Label at a glance#

ProductGeri Protect
Active ingredientPETROLATUM
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 74%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

WARNINGS SECTION

WARNING: FOR EXTERNAL USE ONLY

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

WARNINGS AND PRECAUTIONS SECTION

Caution: Avoid eye contact. If contact - flush eyes thoroughly with water. If local sensitivity develops discontinue use.

DOSAGE & ADMINISTRATION SECTION

Directions: Clean skin. Apply geri-protect ointment, liberally to affected area 2-4 times daily or more frequently as needed.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aloe vera, lanolin, mineral oil, Paraffin wax, PCMX Powder, Phenoxyethanol, Sodium Borate, Vitamins A, D, and E, water deionized, Zinc Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1433743petrolatum 74 % Topical OintmentPSN1
1433743petrolatum 0.74 MG/MG Topical OintmentSCD1
1433743petrolatum 74 % Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54162-650-042020-01-31C16284748780-19d75b9d0-5407-f424-e053-dadaa90a57ceGeri Protect

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54162-650-04Geri Protect118 g in 1 PACKAGEOINTMENT1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54162-650GERI PROTECT (PETROLATUM) OINTMENT [GERITREX LLC]1Legacy NDC, 1 package rows20160101_5ecc1008-7adc-4d12-abcb-a5642ba073cb.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
54162-650-04GM - Gram54162-650a70af7b4-6cd5-4bfb-a381-2417ec7b764412016-01-13

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54162-65054162-650-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UACTIB
ALOE VERA LEAFZY81Z83H0XIACT
LANOLIN7EV65EAW6HIACT
MINERAL OILT5L8T28FGPIACT
PARAFFINI9O0E3H2ZEIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BORATE91MBZ8H3QOIACT
VITAMIN A81G40H8B0TIACT
VITAMIN D9VU1KI44GPIACT
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
CHLOROXYLENOL0F32U78V2QIACT

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
ebe2c61c-a077-4a24-94bb-7af55fb3a15a5ecc1008-7adc-4d12-abcb-a5642ba073cb2015-12-29WarningsExact identifier
spl id: ebe2c61c-a077-4a24-94bb-7af55fb3a15a
spl set id: 5ecc1008-7adc-4d12-abcb-a5642ba073cb

Reported adverse events (FAERS/openFDA)#

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