Geri-Gentle petrolatum

Manufacturer
Geri-gentle corporation
Effective date
2025-01-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:42

Label at a glance#

ProductGeri-Gentle petrolatum
Active ingredientPETROLATUM
Label structure12 sections

Indications and uses

■ helps treat and prevent diaper rash ■ helps seal out wetness ■ temporarily protects minor ■ cuts ■ scrapes ■ burns ■ temporarily helps protect and relieve chapped and cracked skin or lips ■ helps prevent and protect chafed skin or minor skin irritations associated with diaper rash ■ with each diaper change, espicially at bedtime when exposure to wet diapers may be prolonged

Dosage and administration

■ change wet and soiled diapers promptly ■ cleanse the diaper area and allow to dry ■ apply as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

White Petroleum Jelly USP [100% w/w]

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

■ helps treat and prevent diaper rash ■ helps seal out wetness ■ temporarily protects minor ■ cuts ■ scrapes ■ burns ■ temporarily helps protect and relieve chapped and cracked skin or lips ■ helps prevent and protect chafed skin or minor skin irritations associated with diaper rash ■ with each diaper change, espicially at bedtime when exposure to wet diapers may be prolonged

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens ■ symptoms last more than 7 days or clear up and occur again in a few days

Do not use on

OTC - DO NOT USE SECTION

■ deep puncture woulnd ■ animal bites ■ serious burns

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

■ change wet and soiled diapers promptly ■ cleanse the diaper area and allow to dry ■ apply as needed

Other Information

SPL UNCLASSIFIED SECTION

■ store at 59-86F (15-30C) ■ avoid excessive heat

Inactive Ingredient

INACTIVE INGREDIENT SECTION

None

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts and Principal Display PanelDrug Facts and Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204754petrolatum 100 % Topical JellyPSN3
204754petrolatum 1 MG/MG Topical OintmentSCD3
204754petrolatum 100 % Topical JellySY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69771-016-12Geri-Gentle petrolatum5 g in 1 PACKETOINTMENT53
69771-016-14Geri-Gentle petrolatum113 g in 1 TUBEOINTMENT1133

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69771-016GERI-GENTLE PETROLATUM (WHITE PETROLATUM) OINTMENT [GERI-GENTLE CORPORATION]3Current NDC, 2 package rows20250127_0adfbb9e-173c-925a-e063-6394a90aeb5d.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69771-01669771-016-12, 69771-016-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PETROLATUM4T6H12BN9UACTIB

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
Geri-Gentle petrolatumWHITE PETROLATUMGeri-gentle corporation0adfbb9e-173c-925a-e063-6394a90aeb5d2025-01-25WarningsExact identifier
ndc (package): 69771-016-14
ndc (package): 69771-016-12
ndc (product): 69771-016
ndc11 (package): 69771001614
ndc11 (package): 69771001612
spl id: 2c8a2225-540a-8670-e063-6394a90a23b1
spl set id: 0adfbb9e-173c-925a-e063-6394a90aeb5d

Reported adverse events (FAERS/openFDA)#

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