Petroleum Jelly

Manufacturer
Aldermed Inc.
Effective date
2026-05-04
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:56:15

Label at a glance#

ProductPetroleum Jelly
Active ingredientWHITE PETROLATUM
Label structure14 sections

Indications and uses

temporarily protects minor cuts scrapes burns temporarily protects and chafed, chapped or cracked skin helps protect against the drying effects of wind and cold weather

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

White petrolatum USP 100%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily protects minor

  • cuts
  • scrapes
  • burns
  • temporarily protects and chafed, chapped or cracked skin
  • helps protect against the drying effects of wind and cold weather

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 within a few days

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Other information

OTHER SAFETY INFORMATION

  • store at 15°- 30°C (59° to 86° F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

none

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-833-605-84-74 9am-5 pm EST M-F

Distributror

SPL UNCLASSIFIED SECTION

Distributor:
ALDERMED INC.
7901 4TH ST N STE 300 ST PETERSBURG, FL 33702
www.aldermed.us MADE IN INDIA MH/DRUGS/25-KD/739

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204754petrolatum 100 % Topical JellyPSN7
204754petrolatum 1 MG/MG Topical OintmentSCD7
204754petrolatum 100 % Topical JellySY7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87236-009-01Petroleum Jelly28.4 g in 1 TUBEJELLY28.47
87236-009-01Petroleum Jelly1 in 1 CARTONJELLY17
87236-009-02Petroleum Jelly56.6 g in 1 TUBEJELLY56.67
87236-009-04Petroleum Jelly113 g in 1 TUBEJELLY1137
87236-009-05Petroleum Jelly5 g in 1 PACKETJELLY57
87236-009-13Petroleum Jelly368 g in 1 JARJELLY3687
87236-009-15Petroleum Jelly425 g in 1 JARJELLY4257
87236-009-44Petroleum Jelly144 in 1 CARTONJELLY1447
87236-009-44Petroleum Jelly5 g in 1 PACKETJELLY57
87236-009-56Petroleum Jelly56.6 g in 1 TUBEJELLY56.67
87236-009-56Petroleum Jelly1 in 1 CARTONJELLY17

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

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
WHITE PETROLATUMB6E5W8RQJ4ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-03-09monthly-update2026-06-03 17:58:37
52026-02-12monthly-update2026-06-03 17:56:29
22026-01-23monthly-update2026-06-03 17:53:10
12025-12-15monthly-update2026-06-03 17:45:57

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
Petroleum JellyWHITE PETROLATUMAldermed Inc.4e02af41-db86-46d8-a97d-332d84eced6f2026-05-04WarningsExact identifier
ndc (package): 87236-009-44
ndc (package): 87236-009-02
ndc (package): 87236-009-01
ndc (package): 87236-009-56
ndc (package): 87236-009-05
ndc (package): 87236-009-04
ndc (package): 87236-009-15
ndc (package): 87236-009-13
ndc (product): 87236-009
ndc11 (package): 87236000901
ndc11 (package): 87236000905
ndc11 (package): 87236000956
ndc11 (package): 87236000904
ndc11 (package): 87236000913
ndc11 (package): 87236000902
ndc11 (package): 87236000944
ndc11 (package): 87236000915
spl id: 51031aa2-b06f-78c4-e063-6294a90a3d9a
spl set id: 4e02af41-db86-46d8-a97d-332d84eced6f

Reported adverse events (FAERS/openFDA)#

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