BED SORE AND WOUND HEALING CREAM- allantoin cream

Bed Sore and Wound Healing Cream by

Drug Labeling and Warnings

Bed Sore and Wound Healing Cream by is a Otc medication manufactured, distributed, or labeled by TAGRID LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient:

1. Allantoin 0.5%

PURPOSE

1. Skin Protectant

INDICATIONS & USAGE

Uses:

1. Temporarily protects minor cuts, scrapes, and burns
2. Helps relieve skin irritation associated with bed sores, pressure ulcers, or cracked skin
3. Aids in the healing of wounds by forming a protective moisture barrier

WARNINGS

For external use only

Do not use:

• On deep or puncture wounds
• On animal bites
• On serious burns

Ask a doctor before use if you have:

A serious wound or condition that requires medical attention

When using this product

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

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
• You are allergic to any of the ingredients in this product

If pregnant or breast-feeding

Ask a health professional before use

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions:

• Clean the affected area
• Apply a thin layer to the affected area 2 to 3 times daily or as directed by a physician
• May be covered with a sterile bandage or left uncovered

OTHER SAFETY INFORMATION

Other information:

• Store at 15°–30°C (59°–86°F)
• Avoid freezing and direct sunlight
• Tamper-evident: Do not use if seal under cap is broken or missing

INACTIVE INGREDIENT

Inactive ingredients:

• Colloidal Silver
• Water
• Tocopherol
• Madecassoside
• Centella Asiatica Whole
• Sodium Hyaluronate
• Honey
• Polysorbate 60
• Cetearyl Alcohol
• Mineral Oil
• White Petrolatum
• Glycerin
• Lavandula Angustifolia (Lavender) Oil

QUESTIONS

Questions or comments?

Contact us at support@tagridstore.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BED SORE AND WOUND HEALING CREAM 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85384-0011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
COLLOIDAL SILVER (UNII: 3M4G523W1G)
WATER (UNII: 059QF0KO0R)
TOCOPHEROL (UNII: R0ZB2556P8)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
HONEY (UNII: Y9H1V576FH)
POLYSORBATE 60 (UNII: CAL22UVI4M)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
MINERAL OIL (UNII: T5L8T28FGP)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
GLYCERIN (UNII: PDC6A3C0OX)
LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85384-0011-1	30 g in 1 TUBE; Type 0: Not a Combination Product	06/11/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	06/11/2025

Labeler - TAGRID LLC (118778969)

Registrant - TAGRID LLC (118778969)