A+D Medicated Rash Ointment

Manufacturer
WellSpring Pharmaceutical Corporation
Effective date
2024-12-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
weekly-update
Hydrated at
2026-07-17 21:43:46

Label at a glance#

ProductAD Medicated Rash
Active ingredientMINERAL OIL, OATMEAL
Label structure10 sections

Indications and uses

Temporarily protects and helps relieve minor skin irritation and itching due to: rashes eczema

Dosage and administration

apply as needed

Storage and handling

store between 20° to 25°C (68° to 77°F)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Mineral Oil 30%

Colloidal Oatmeal 2%

Purpose 

OTC - PURPOSE SECTION

Skin protectant

Skin protectant

Uses

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve minor skin irritation and itching due to:

  • rashes
  • eczema

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 worsens
  • symptoms persist for more than 7 days, or clear up and occur again within a few days

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

Other information

STORAGE AND HANDLING SECTION

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Paraffin, Microcrystalline Wax, Euphorbia Cerifera (Candelilla) Wax, Lanolin,Fragrance (Parfum), Glycerin, Cod Liver Oil (contains vitamin A & vitamin D), Water,
Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Potassium Sorbate, Sorbic Acid.

Questions?

OTC - QUESTIONS SECTION

1-844-241-5454 or ADskinhealth.com

Distributed by:

SPL UNCLASSIFIED SECTION

WellSpring Pharmaceutical Corporation
Sarasota, FL 34243

© 2024 WellSpring Pharmaceutical Corporation

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL  65197-406-15

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

A+D Medicated Rash Ointment

SOOTHES, PROTECTS, RELIEVES RASH AND IRRITATED SKIN

WITH VITAMIN A & VITAMIN D plus COLLOIDAL OATMEAL & EUCALYPTUS

PARABEN-FREE
DYE-FREE
PHTHALATE-FREE

NET WT 1.5 OZ (42.5g)

Skin nourishing formula with Vitamin A and Vitamin D

helps heal and moisturize irritated skin

CLINICALLY PROVEN TO IMPROVE:

Itching

Stinging

Irritated Skin

Redness

Dryness

CT40600B

NDC# 65197-406-15

UPC: 365197406005

CT40600B
CT40600B

65197-406-52

SPL UNCLASSIFIED SECTION

A+D Medicated Rash Ointment 15.2 ozA+D Medicated Rash Ointment 15.2 oz65197-406-52

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqrco.de/bfBtrHad-medicated-rash-ointment-1.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65197-40665197-406-15, 65197-406-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-12-27full-release2026-06-01 00:59:47

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
AD Medicated RashAD MEDICATED RASHWellSpring Pharmaceutical Corporationaac345bf-ea66-4f5b-a497-c24ea72f93ea2024-12-27WarningsExact identifier
ndc (package): 65197-406-15
ndc (package): 65197-406-52
ndc (product): 65197-406
ndc11 (package): 65197040652
ndc11 (package): 65197040615
spl id: 8fd6a4a0-06b0-4006-b00c-b910dfeb6d7b
spl set id: aac345bf-ea66-4f5b-a497-c24ea72f93ea

Reported adverse events (FAERS/openFDA)#

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