AD MEDICATED RASH ointment

AD Medicated Rash by

Drug Labeling and Warnings

AD Medicated Rash by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Mineral Oil 30%

Colloidal Oatmeal 2%

Purpose 

Skin protectant

Skin protectant

Uses

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

• rashes
• eczema

Warnings

For external use only

When using this product

• do not get into 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

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply as needed

Other information

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

Inactive ingredients

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?

1-844-241-5454 or ADskinhealth.com

Distributed by:

WellSpring Pharmaceutical Corporation
Sarasota, FL 34243

© 2024 WellSpring Pharmaceutical Corporation

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL  65197-406-15

A+D MEDICATED RASH OINTMENT 1.5oz

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

 

CT40600A

P13018.00

NDC# 65197-406-15

UPC: 365197406005

INGREDIENTS AND APPEARANCE

AD MEDICATED RASH 
ad medicated rash ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65197-406
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP)	MINERAL OIL	30 g  in 100 g
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
PARAFFIN (UNII: I9O0E3H2ZE)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
CANDELILLA WAX (UNII: WL0328HX19)
LANOLIN (UNII: 7EV65EAW6H)
GLYCERIN (UNII: PDC6A3C0OX)
COD LIVER OIL (UNII: BBL281NWFG)
WATER (UNII: 059QF0KO0R)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CHAMOMILE (UNII: FGL3685T2X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SORBIC ACID (UNII: X045WJ989B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-406-15	1 in 1 BOX	01/15/2025
1		42.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/15/2025

Labeler - WellSpring Pharmaceutical Corporation (110999054)