equate

Manufacturer
Wal-Mart Stores Inc
Effective date
2017-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:11

Label at a glance#

Productequate ECZEMA RELIEF
Active ingredientOATMEAL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Colloidal oatmeal 2%

OTC - PURPOSE SECTION

Purpose

Skin protectant

INDICATIONS & USAGE SECTION

Uses  temporarily protects and helps relieve minor skin

irritation and itching due to  •eczema  •rashes

WARNINGS SECTION

Warnings

For external use only.

When using this product •avoid contact with eyes

Stop use and ask a doctor if condition worsens •symptoms

persist for more than 7 days or clear up and

occur again within a few days.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

apply to affected areas of skin as needed

INACTIVE INGREDIENT SECTION

Inactive ingredients water, glycerin, propanediol,

dimethicone, petrolatum, glyceryl stearate, cetyl alcohol,

aloe barbadensis leaf juice, jojoba esters, polyacrylamide, C13-14

isparaffin, laureth-7, butyrosperum parkii (shea) butter extract, avena sativa

(oat) kernel extract, bisabolol, zingiber officinale (ginger) root extract, c10-30

cholesterol/ lanosterol esters, ceramide, NG, hydrolyzed jojoba esters,

tocopheryl acetate, magnesium ascorbyl phosphate, panthenol,

ethylhexylglycerin, c12-15 alkyl benzoate, tribehenin, potassium hydroxide,

disodium EDTA, phenoxyethanol, PEG-10 phytosterol, palmitoyl hexapeptide-

12

OTC - QUESTIONS SECTION

Satisfaction guaranteed -  For questions or

comments please call 1-888-287-1915

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-614-082023-08-02C16284748780-1f386c64a-480b-0266-e053-dadaa90a7c1abe440cb5-e5b6-4fd3-a058-563d72893b12
49035-614-082023-01-30C16284748780-1f386c64a-480b-0266-e053-dadaa90a7c1abe440cb5-e5b6-4fd3-a058-563d72893b12

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-61449035-614-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

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
018e541a-09ea-592c-e063-6294a90a0a30be440cb5-e5b6-4fd3-a058-563d72893b122023-07-28WarningsExact identifier
spl set id: be440cb5-e5b6-4fd3-a058-563d72893b12

Reported adverse events (FAERS/openFDA)#

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