HYDRATING HEALING

Manufacturer
RITE AID
Effective date
2010-07-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:15

Label at a glance#

ProductHYDRATING HEALING DAILY THRAPY
Active ingredientPETROLATUM
Label structure4 sections

Indications and uses

USES: TEMPORARILY PROTECTS MINOR 'CUTS' SCRAPS 'BURNS TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN AND LIPS HELPS PROTECT FROM THE DRYING EFFECTS OF COLD WIND AND WEATHER DIRECTIONS: APPLY AS REQUIRED.

Dosage and administration

USES: TEMPORARILY PROTECTS MINOR 'CUTS' SCRAPS 'BURNS TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN AND LIPS HELPS PROTECT FROM THE DRYING EFFECTS OF COLD WIND AND WEATHER DIRECTIONS: APPLY AS REQUIRED.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

  • PETROLATUM 41% ( SKIN PROTECTANT)

USES AND DIRECTIONS

OTC - PURPOSE SECTION

USES:
  • TEMPORARILY PROTECTS MINOR 'CUTS' SCRAPS 'BURNS
  • TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN AND LIPS
  • HELPS PROTECT FROM THE DRYING EFFECTS OF COLD WIND AND WEATHER
DIRECTIONS: APPLY AS REQUIRED.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYE THOROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

OTC - STOP USE SECTION

CONDITION WORSENS OR SYMPTOMS PERSIST FOR MORE THAN SEVEN DAYS, OR OCCUR AGAIN WITHIN FEW DAYS.

DO NOT USE

OTC - DO NOT USE SECTION

  • ON DEEP OR PUNCTURED WOUNDS, OR ON ANIMAL BITE, OR ON SERIOUS BURNS
  • IF INNER SEAL IS MISSING OR BROKEN

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2oz front and back labels:

ra2f.jpg2OZ FRONT LABEL2OZ FRONT LABEL

ra2b.jpg2OZ BACK LABEL2OZ BACK LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
725145petrolatum 41 % Topical OintmentPSN1
725145petrolatum 0.41 MG/MG Topical OintmentSCD1
725145petrolatum 41 % Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-3300-22020-01-31C16284748780-19d75b9d0-7c57-f424-e053-dadaa90a57ceDRUG FACTS BOX (BACK LABEL)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-3300-2HYDRATING HEALINGDAILY THRAPY56 g in 1 TUBEOINTMENT561

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-3300HYDRATING HEALING DAILY THRAPY (PETROLATUM) OINTMENT [RITE AID]1Legacy NDC, 1 package rows20100719_43a835ec-d9a5-46a4-8c2d-eccbea3d5053.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
PETROLATUMACTIVE MOIETY4T6H12BN9U1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-330011822-3300-2

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
38a19499-c16a-41ce-b296-46d8e9294f7443a835ec-d9a5-46a4-8c2d-eccbea3d50532010-07-19WarningsExact identifier
spl id: 38a19499-c16a-41ce-b296-46d8e9294f74
spl set id: 43a835ec-d9a5-46a4-8c2d-eccbea3d5053

Reported adverse events (FAERS/openFDA)#

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