THE MAN BY VANIBISS RAZOR BUMPS SERUM- allantoin gel

THE MAN BY VANIBISS RAZOR BUMPS SERUM by

Drug Labeling and Warnings

THE MAN BY VANIBISS RAZOR BUMPS SERUM by is a Otc medication manufactured, distributed, or labeled by Vanibiss Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Allantoin 0.5%

PURPOSE

Skin Protectant

USE

Temporarily protects and helps relieve chapped or cracked skin.

WARNINGS

For external use only.

Do not use on children under 12 years of age unless directed by a doctor.

WHEN USING

do not get into eyes.

STOP USE

Condition worsens.

Symptoms last more than 7 days or clear up and occur again within a few days.

DO NOT USE

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 on the affected area as needed.

OTHER SAFETY INFORMATION

See on the bottom of the container for lot number and expiration date.

Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT

Water (Aqua), Propylene Glycol, Glycerin, Salicylic Acid, Polysorbate 20, Silica, Xanthan Gum, Fragrance (Parfum), Salix Alba (Willow) Bark Extract, Sodium Hydroxide, Benzyl Alcohol, Benzoic Acid, Sorbic Acid, Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Alpha-Isomethyl Ionone, Geraniol, Linalool, Eugenol.

QUESTIONS OR COMMENTS?

Call (1-800-931-0171)

THE MAN BY VANIBISS RAZOR BUMPS SERUM BOX

THE MAN BY VANIBISS RAZOR BUMPS SERUM ROLL ON

INGREDIENTS AND APPEARANCE

THE MAN BY VANIBISS RAZOR BUMPS SERUM 
allantoin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81890-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SALICYLIC ACID (UNII: O414PZ4LPZ)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
EUGENOL (UNII: 3T8H1794QW)
BENZOIC ACID (UNII: 8SKN0B0MIM)
SORBIC ACID (UNII: X045WJ989B)
BENZYL ALCOHOL (UNII: LKG8494WBH)
WILLOW BARK (UNII: S883J9JDYX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
COUMARIN (UNII: A4VZ22K1WT)
GERANIOL (UNII: L837108USY)
GLYCERIN (UNII: PDC6A3C0OX)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81890-005-03	1 in 1 BOX	02/15/2024
1		103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	02/15/2024

Labeler - Vanibiss Inc (104730560)