Label: SEROMEN RAZOR BUMPS- allantoin gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 10, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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 (1-877-737-6267)

  • SEROMEN RAZOR BUMPS SOLUTION BOX

    RAZOR BUMPS BOX

  • SEROMEN RAZOR BUMPS SOLUTION ROLL ON

    RAZOR BUMPS TUBE

  • INGREDIENTS AND APPEARANCE
    SEROMEN RAZOR BUMPS 
    allantoin gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82767-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82767-005-031 in 1 BOX06/10/2024
    1103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01606/10/2024
    Labeler - TEAMTRADE INC. (067321781)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!