Relief Soothing Bath Treatment

Manufacturer
Blue Cross Laboratories, Inc.
Effective date
2022-11-15
Label type
HUMAN OTC DRUG LABEL
Version
24
Source
full-release
Hydrated at
2026-05-31 23:51:33

Label at a glance#

ProductRelief Soothing Bath Treatment
Active ingredientOATMEAL
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each packet)                      Purpose

colloidal oatmeal, 100%                                    Skin protectant

OTC - PURPOSE SECTION

Uses    Temporarily protects and relieves minor skin irritation and itching due to one or more of the following

rashes

eczema

insect bites

sunburn

poison ivy, oak, or sumac

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.

INDICATIONS & USAGE SECTION

When using this product

do not get into eyes

in some skin conditions, soaking too long may overdry

to avoid slipping, use mat in tub or shower

WARNINGS SECTION

Warning For external use only

DOSAGE & ADMINISTRATION SECTION

Directions
Turn warm water faucet on to full force.
Slowly sprinkle one packet of colloidal oatmeal directly into tub or container.
stir any colloidal oatmeal that may have settled at the bottom.
soak affected area for 15-30 minutes as needed or as directed by a doctor.
pat dry (do not rub) to keep a thin layer on the skin.

INACTIVE INGREDIENT SECTION

No inactive ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Relief

Soothing Bath Treatment

6 single use packets

Total net Wt. 9 oz. (255g)

boxbox

bagbag

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OATMEAL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20181113

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
22431-359-032024-01-30C16284748780-1d6a99b39-9f93-a426-e053-dadaa90af4c2Soothing Bath Treatment
22431-359-022022-03-14C16284748780-1d6a99b39-9f93-a426-e053-dadaa90af4c2Soothing Bath Treatment
22431-359-022022-01-28C16284748780-1d6a99b39-9f93-a426-e053-dadaa90af4c2Soothing Bath Treatment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
22431-359-01Relief Soothing Bath Treatment42.5 g in 1 PACKETGRANULE, EFFERVESCENT42.524
22431-359-02Relief Soothing Bath Treatment6 in 1 BOXGRANULE, EFFERVESCENT624
22431-359-03Relief Soothing Bath Treatment3 in 1 BOXGRANULE, EFFERVESCENT324

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
22431-359RELIEF SOOTHING BATH TREATMENT (COLLOIDAL OATMEAL) GRANULE, EFFERVESCENT [BLUE CROSS LABORATORIES, INC.]24Legacy NDC, 3 package rows20221116_d8deb0ff-1d5f-41e3-919f-d6c4ef9810ce.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OATMEALACTIVE INGREDIENT8PI54V663Y18
OATMEALACTIVE MOIETY8PI54V663Y18

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
22431-35922431-359-01, 22431-359-02, 22431-359-03

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
OATMEAL8PI54V663YACTIB

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
ed860819-987a-ae24-e053-2a95a90afa5ad8deb0ff-1d5f-41e3-919f-d6c4ef9810ce2022-11-15WarningsExact identifier
spl id: ed860819-987a-ae24-e053-2a95a90afa5a
spl set id: d8deb0ff-1d5f-41e3-919f-d6c4ef9810ce

Reported adverse events (FAERS/openFDA)#

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