SKIN PROTECTANT WITH 33% PETROLATUM ADVANCE MOISTURIZING CREAM- petrolatum cream

Skin Protectant with 33% Petrolatum by

Drug Labeling and Warnings

Skin Protectant with 33% Petrolatum by is a Otc medication manufactured, distributed, or labeled by Aldermed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Petrolatum 33%

Purpose

Skin Protectant

Use(s)

Temporarily protects and helps relieve dry, chapped, or cracked skin

Helps protect skin from the drying effects of wind and cold weather

Warnings

For External Use Only

Do not get into eyes

Stop use and ask a doctor if

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

Do not use

On deep puncture wounds Animal bites Serious burns.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Apply as needed 

Other information

Store at room temperature 15º-30ºC (59° - 86°F)

Tamper evident. Do not use if seal is damaged.

Inactive Ingredients

DMDM Hydantoin, Lanolin Alcohol, Methyl Paraben, Mineral Oil, Paraffin, PEG 30 Dipolyhydroxystearate, Propylene Glycol, Propylparaben, Purified Water, Sodium Chloride

Questions?

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Label

label

INGREDIENTS AND APPEARANCE

SKIN PROTECTANT WITH 33% PETROLATUM   ADVANCE MOISTURIZING CREAM
petrolatum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	33 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
PARAFFIN (UNII: I9O0E3H2ZE)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
DMDM HYDANTOIN (UNII: BYR0546TOW)
MINERAL OIL (UNII: T5L8T28FGP)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-011-37	106 g in 1 TUBE; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/01/2025

Labeler - Aldermed Inc. (144887712)

Registrant - Aldermed Inc. (144887712)