Princess Petroleum

Manufacturer
Ultra Distributors Inc. | Jell Pharmaceuticals Pvt. Ltd.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:44:41

Label at a glance#

ProductPrincess Petroleum
Active ingredientPETROLATUM
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

White petrolatum USP (100%)

OTC - PURPOSE SECTION

Purpose

Skin protectant

INDICATIONS & USAGE SECTION

Uses

helps protect chapped skin

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product

  • do not get into eyes

OTC - ASK DOCTOR SECTION

See a doctor ifcondition lasts more than 7 days.

OTC - DO NOT USE SECTION

Do not use on

  • deep or puncture wounds
  • 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.

DOSAGE & ADMINISTRATION SECTION

Directions

apply as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

None

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCESS PETROLEUM JELLY

NET WT 6 OZ (170 gm)

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204754petrolatum 100 % Topical JellyPSN2
204754petrolatum 1 MG/MG Topical OintmentSCD2
204754petrolatum 100 % Topical JellySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78495-004-01Princess Petroleum113 g in 1 JARJELLY1132
78495-004-02Princess Petroleum170 g in 1 JARJELLY1702
78495-004-03Princess Petroleum226 g in 1 JARJELLY2262
78495-004-04Princess Petroleum368 g in 1 JARJELLY3682

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78495-004PRINCESS PETROLEUM (WHITE PETROLATUM) JELLY [ULTRA DISTRIBUTORS INC.]2Current NDC, Legacy NDC, 4 package rows20241220_6d9c92bf-9263-40a4-acac-5c3f0b08c69d.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78495-00478495-004-01, 78495-004-02, 78495-004-03, 78495-004-04

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
Princess PetroleumWHITE PETROLATUMUltra Distributors Inc.6d9c92bf-9263-40a4-acac-5c3f0b08c69d2024-12-18WarningsExact identifier
ndc (package): 78495-004-01
ndc (package): 78495-004-03
ndc (package): 78495-004-02
ndc (package): 78495-004-04
ndc (product): 78495-004
ndc11 (package): 78495000402
ndc11 (package): 78495000401
ndc11 (package): 78495000403
ndc11 (package): 78495000404
spl id: 298dabf6-4ce8-7ed2-e063-6394a90a1bdc
spl set id: 6d9c92bf-9263-40a4-acac-5c3f0b08c69d

Reported adverse events (FAERS/openFDA)#

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