PURESKIN BED AND PRESSURE SORE- allantoin cream

Pureskin Bed and Pressure Sore by

Drug Labeling and Warnings

Pureskin Bed and Pressure Sore by is a Otc medication manufactured, distributed, or labeled by BENLONG HALL LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active ingredient

Allantoin 0.6%

Purpose

Skin protectant

Uses

• helps prevent and temporarily protects chafed, chapped or cracked skin
• helps protect from the drying effects of wind and cold weather

Warnings

​For external use only.

When using this product

do not get into eyes

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

• deep or puncture wounds
• animal bites
• serious burns

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 at room temperature

Inactive ingredients

Water, Beeswax, Jojoba Oil, Coconut Oil, Medium-Chain Triglycerides (MCT Oil), Panax Notoginseng Extract (Panax Notoginseng Root), Lithospermum Root Extract (Lithospermum Erythrorhizon Root), Honeysuckle Flower Extract (Lonicera Japonica Flower), Calendula Extract (Calendula Officinalis Flower), Immortelle (Helichrysum) Extract (Helichrysum Italicum Flower), Phellodendron Bark Extract (Phellodendron Amurense Bark), Centella Asiatica Extract (Centella Asiatica Triterpenoids), Chamomile Extract (Matricaria Chamomilla Whole), Bisabolol (Alpha-Bisabolol (+/-)), Tremella Polysaccharide (Tremella Fuciformis Whole), Geniposide, Matrine (Sophora Flavescens Alkaloid), Panthenol (Vitamin B5), Vitamin E (Tocopherol), Glycerin, Hydroxyacetophenone.

Principal Display Panel

INGREDIENTS AND APPEARANCE

PURESKIN BED AND PRESSURE SORE 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87217-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LITHOSPERMUM ERYTHRORHIZON ROOT (UNII: 9I70D8O47I)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
GENIPOSIDE (UNII: 145295QLXY)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
MATRINE (UNII: N390W430AC)
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BEESWAX (UNII: 2ZA36H0S2V)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
JOJOBA OIL (UNII: 724GKU717M)
COCONUT OIL (UNII: Q9L0O73W7L)
PANTHENOL (UNII: WV9CM0O67Z)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87217-001-01	141 g in 1 JAR; Type 0: Not a Combination Product	12/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/16/2025

Labeler - BENLONG HALL LLC (116207764)