PROCURE HYDROSHIELD- petrolatum 44.28% ointment

ProCure HydroShield by

Drug Labeling and Warnings

ProCure HydroShield by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient: Petrolatum 44.28%

Purpose

Purpose: Skin Protectant

Uses

Uses

• Temporarily protects minor: cuts, scrapes, burns
• Temporarily protects and helps relieve chafed, chapped or cracked skin and lips
• Helps protect from the drying effects of wind and cold weather

Warnings

Warnings

For external use only

When using this product

When using this product do not get into the eyes

Stop use and ask a doctor if

Stop use and ask a doctor if

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

Do not use on

Do not use on deep or puncture wounds, animal bites, serious burns

Keep out of reach of children

Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away

Directions

Directions: Apply as needed

Inactive Ingredients

Inactive Ingredients

Mineral Oil, Microcrystalline Wax, Paraffin, Lanolin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE HYDROSHIELD 
petrolatum 44.28% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	44.28 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
PARAFFIN (UNII: I9O0E3H2ZE)
MINERAL OIL (UNII: T5L8T28FGP)
LANOLIN (UNII: 7EV65EAW6H)

Product Characteristics
Color	white (White to slightly yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-034-04	106 g in 1 TUBE; Type 0: Not a Combination Product	09/15/2025
2	NDC: 55681-034-16	453 g in 1 JAR; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/15/2025

Labeler - Twin Med LLC (009579330)