FDA.reportPublic FDA data

PHARMACYS PRESCRIPTION CREAMY PETROLEUM COCOA BUTTER

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2022-10-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:05

Label at a glance#

ProductPHARMACYS PRESCRIPTION CREAMY PETROLEUM COCOA BUTTER
Active ingredientPETROLATUM
Label structure8 sections

Indications and uses

Temporarily protects minor: cuts, scrapes, burns. Temporarily protects and helps relieve chapped or cracked skin. Helps protect from the drying effects of wind and cold weather.

Dosage and administration

apply as needed.

Label contents#

Full prescribing information#

Drug Facts Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 30%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Temporarily protects minor: cuts, scrapes, burns.

Temporarily protects and helps relieve chapped or cracked skin.

Helps protect from the drying effects of wind and cold weather.

Warnings

WARNINGS SECTION

For external use only.

When using this product do not get into eyes.

Stop use and ask a doctor if: condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

Do not use on: deep puncture wounds, animal bites, serious burns.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (aqua), Mineral Oil, Glycerin, Cetearyl Alcohol, Cetyl Alcohol, Stearyl Alcohol, Glyceryl Stearate, Fragrance, Polysorbate 80, Laureth-20, BHT, Methylparaben, Propylparaben, Dimethicone, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-12276176-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UACTIB
WATER059QF0KO0RIACT
MINERAL OILT5L8T28FGPIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERYL STEARATE/PEG-100 STEARATERD25J5V947IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARYL ALCOHOL2KR89I4H1YIACT
GLYCERINPDC6A3C0OXIACT
METHYLPARABENA2I8C7HI9TIACT
DIMETHICONE92RU3N3Y1OIACT
POLYSORBATE 806OZP39ZG8HIACT
LAURETH-206SU0SC83AHIACT
PROPYLPARABENZ8IX2SC1OHIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
COCOA BUTTER512OYT1CRRIACT

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
ebc33e4a-aff5-a326-e053-2a95a90a08c19c3a841e-ffb5-2d20-e053-2a95a90aea352022-10-24WarningsExact identifier
spl id: ebc33e4a-aff5-a326-e053-2a95a90a08c1
spl set id: 9c3a841e-ffb5-2d20-e053-2a95a90aea35

Reported adverse events (FAERS/openFDA)#

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