skin protectant

Manufacturer
Great Lakes Wholesale Marketing and Sales, Inc | Illinois Industrial Tool, Inc | Ningbo Liyuan Chemical Products co., Ltd
Effective date
2016-08-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:23:00

Label at a glance#

Productskin protectant Cocoa Butter
Active ingredientPETROLATUM
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

GLS PERSONAL CARE SOLUTIONS

Cocoa Butter Petroleum Jelly

Vitamin E

Skin Protectant

With Extra Rich Cocoa Butter

Tones, softens & smooths dry skin

4.5 fl. o (133 ml)

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

White Petroleum Purpose

Petrolatum 30%....................................................................Skin Protectant

OTC - PURPOSE SECTION

Skin Protectant Lotion

INDICATIONS & USAGE SECTION

  • Temporarily protect minor cuts, scrapes, & burns
  • Temporarily protects and helps relieve chapped or cracked skin
  • Helps protect from the drying efffects of wind and cold weather

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INSTRUCTIONS FOR USE SECTION

Apply as needed.

DOSAGE & ADMINISTRATION SECTION

Topical skin protectant lotion

30% Petrolatum

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 cocao (cocoa) seed butter, tocopheryl acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cocoa Butter Petroleum JellyCocoa Butter Petroleum Jelly

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64092-254-042023-01-30C16284748780-1f386c649-c3f6-0266-e053-dadaa90a7c1a395a97cb-45f0-0757-e054-00144ff8d46c

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
64092-25464092-254-04

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
PETROLATUM4T6H12BN9UACTIB
WATER059QF0KO0RIACT

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
3b4bf826-51e8-4d71-e054-00144ff8d46c395a97cb-45f0-0757-e054-00144ff8d46c2016-08-30WarningsExact identifier
spl id: 3b4bf826-51e8-4d71-e054-00144ff8d46c
spl set id: 395a97cb-45f0-0757-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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