Label: DYNAMIC DRYING- calamine 15% and zinc oxide 2% lotion

  • NDC Code(s): 79849-001-01
  • Packager: Guangzhou Xiran Cosmetics Co.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 28, 2022

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

View All Sections
  • Active Ingredients

    Calamine 15%

    Zinc Oxide 2%

  • Purpose

    Astringent

    Astringent

  • Uses

    Temporally relieves minor skin irritations

  • Warnings

    For External Use only

  • When using this product

    Avoid contact with eyes

    If contact occurs, rinse thoroughly with water

    In some skin conditions, soaking too long may over dry.

  • Stop use and ask a doctor if

    Condition worsens or symptoms last more than 7 days

  • Keep out of reach of children.

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

  • Directions

    Apply to the affected area as often as necessary

  • Inactive Ingredients

    Isopropyl Alcohol, Water, Glycerin, Titanium Dioxide, Talc, Salicylic Acid, Sulfur, Camphor

  • Questions or Comments?

    PO BOX 230258 Brooklyn, NY 11223

  • Dynamic Drying Lotion

    label

  • INGREDIENTS AND APPEARANCE
    DYNAMIC DRYING 
    calamine 15% and zinc oxide 2% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79849-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION170 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TALC (UNII: 7SEV7J4R1U)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    CAMPHOR, (-)- (UNII: 213N3S8275)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    SULFUR (UNII: 70FD1KFU70)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79849-001-0129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/01/202006/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34707/01/202006/10/2024
    Labeler - Guangzhou Xiran Cosmetics Co.,Ltd (541581239)
    Registrant - Global Beauty Care, Inc (068600947)
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!