FDA.reportPublic FDA data

Rite Aid

Manufacturer
Rite Aid Corporation
Effective date
2016-05-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:26:55

Label at a glance#

ProductRite Aid
Active ingredientPETROLATUM
Label structure9 sections

Storage and handling

Other information   -store at room temperature

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Petrolatum, 41%

OTC - PURPOSE SECTION

Purpose

Skin protectant (ointment)

INDICATIONS & USAGE SECTION

Uses  -temporarily protects and helps relieve chapped or cracked skin and lips

-temporarily prtects minor:  -cuts  -scrapes  -burns  -helps protect from the drying effects of

wind and cold weather  -helps treat and prevent diaper rash

WARNINGS SECTION

Warnings

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 or puncture wounds  -animal bites  -serious burns

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control

Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions  -apply as needed

STORAGE AND HANDLING SECTION

Other information  -store at room temperature

INACTIVE INGREDIENT SECTION

Inactive ingredients  mineral oil, ceresin, lanolin alcohol, glycerin,

panthenol (pro-vitamin B5), bisabolol, hippophae

rhamnoides oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-5211-62023-08-02C16284748780-1f386c64a-2327-0266-e053-dadaa90a7c1aaeb2afa9-05c9-4d17-94d9-1d7bb0915e82
11822-5211-62023-01-30C16284748780-1f386c64a-2327-0266-e053-dadaa90a7c1aaeb2afa9-05c9-4d17-94d9-1d7bb0915e82

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-521111822-5211-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UACTIB
MINERAL OILT5L8T28FGPIACT
CERESINQ1LS2UJO3AIACT
LANOLIN ALCOHOLS884C3FA9HEIACT
GLYCERINPDC6A3C0OXIACT
PANTHENOLWV9CM0O67ZIACT
LEVOMENOL24WE03BX2TIACT
HIPPOPHAE RHAMNOIDES SEED OILT53SBG6741IACT

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
018e11ca-b27c-9d94-e063-6294a90a3df2aeb2afa9-05c9-4d17-94d9-1d7bb0915e822023-07-28WarningsExact identifier
spl set id: aeb2afa9-05c9-4d17-94d9-1d7bb0915e82

Reported adverse events (FAERS/openFDA)#

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