SUPRADERM- white petrolatum, lanolin cream

SUPRADERM by

Drug Labeling and Warnings

SUPRADERM by is a Otc medication manufactured, distributed, or labeled by Olen Skin Care Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients

30% White Petrolatum

15% Lanolin

PURPOSE

Purpose

Skin Protectant

INDICATIONS & USAGE

Uses

Temporarily Protects Minor:

• Cuts
• Scrapes
• Burns
• Temporarily protects and helps relieve chapped or cracked skin
• Helps protect from the drying effects of wind and cold weather

WARNINGS

Warnings

For External Use Only

WHEN USING

When using this product

• Do not get into eyes

ASK DOCTOR

Stop use and ask a doctor if

• Condition worsens
• Symptoms last more that 7 days or clear up and occur again within a few days

DO NOT USE

Do not use on

• Deep or puncture wounds
• Animal bites
• Serious burns

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed, get medical help or contact a Poison control Center right away.

DOSAGE & ADMINISTRATION

Directions

Apply liberally to affected area of the skin as needed.

STORAGE AND HANDLING

Other information

Store between 59-86°F

INACTIVE INGREDIENT

Inactive ingredients

zinc oxide, corn starch

QUESTIONS

Questions? 1-877-494-4313

PRINCIPAL DISPLAY PANEL

SUPRADERM

Skin Protectant

Barrier & Healing Cream

100% NATURAL

HYPOALLERGENIC

NDC: 52358-0002-3

NET WT 16 OZ.

INGREDIENTS AND APPEARANCE

SUPRADERM 
white petrolatum, lanolin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52358-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	0.3 g  in 1 g
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	0.15 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ZINC OXIDE (UNII: SOI2LOH54Z)
STARCH, CORN (UNII: O8232NY3SJ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52358-0002-1	113 g in 1 JAR; Type 0: Not a Combination Product	11/02/2015
2	NDC: 52358-0002-2	340 g in 1 JAR; Type 0: Not a Combination Product	11/02/2015
3	NDC: 52358-0002-3	454 g in 1 JAR; Type 0: Not a Combination Product	11/02/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	10/17/2014

Labeler - Olen Cosmetics Corporation (250916611)