FDA.reportPublic FDA data

DG BODY

Manufacturer
DOLGENCORP INC | APOLLO HEALTH AND BEAUTY CARE
Effective date
2015-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:53

Label at a glance#

ProductDG BODY PETROLEUM COCOA BUTTER
Active ingredientPETROLATUM
Label structure7 sections

Dosage and administration

APPLY AS NEEDED

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

PETROLATUM 99.8%

PURPOSE

OTC - PURPOSE SECTION

SKIN PROTECTANT

USE

INDICATIONS & USAGE SECTION

HELPS PROTECT CHAPPED SKIN

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 LASTS MORE THAN 7 DAYS

DO NOT USE ON

OTC - DO NOT USE SECTION

  • 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

FRAGRANCE (PARFUM), THEOBROMA CACAO (COCOA) SEED BUTTER

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

1-888-309-9030

LABEL COPY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IMAGE OF THE LABELIMAGE OF THE LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1100455petrolatum 99.8 % Topical GelPSN1
1100455petrolatum 0.998 MG/MG Topical GelSCD1
1100455petrolatum 99.8 % Topical GelSY1
1100455petrolatum 99.8 % Topical JellySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55910-317-082020-01-31C16284748780-19d75b9d0-8746-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55910-317-08DG BODYPETROLEUM COCOA BUTTER212 g in 1 JARJELLY2121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-317DG BODY PETROLEUM COCOA BUTTER (PETROLATUM) JELLY [DOLGENCORP INC]1Legacy NDC, 1 package rows20150305_62be11df-82ce-4cb5-9285-0431c836d702.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
COCOA BUTTERINACTIVE INGREDIENT512OYT1CRR1

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
55910-31755910-317-08

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
COCOA BUTTER512OYT1CRRIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
COCOA BUTTERCOCOA BUTTER512OYT1CRRSUPPOSITORY / RECTAL2280 mgExact identifier — unii candidate

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
08ce697e-17f4-46b5-a1ac-efa053da815f62be11df-82ce-4cb5-9285-0431c836d7022015-02-27WarningsExact identifier
spl id: 08ce697e-17f4-46b5-a1ac-efa053da815f
spl set id: 62be11df-82ce-4cb5-9285-0431c836d702

Reported adverse events (FAERS/openFDA)#

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