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Glizigen Gel Intimate

Medically reviewed by Drugs.com. Last updated on Mar 8, 2021.

Dosage form: gel
Ingredients: GLYCERIN 0.5mg in 1mL
Labeler: Catalysis, SL
NDC Code: 64539-017

Glizigen Intimate Gel

Glycerin 0.5%...................Skin Protectant

  • Stop use and ask a doctor if rash occurs
  • Children under 6 months: ask a doctor

  • Keep out of reach of children

  • For external use only.
  • Do not use on damaged or broken skin.
  • When using this product keep our of the eyes. Rinse with water to remove.
  • Stop use and ask a doctor if rash occurs.
  • Keep out of reach of children
  • Children under 6 months: as a doctor.

  • Apply a small amount the intimate parts and gently wash. Rinse with water
  • Maybe used as often as necessary

  • Apply a small amount the intimate parts and gently wash. Rinse with water
  • Maybe used as often as necessary

  • Stop use and ask a doctor if rash occurs
  • Children under 6 months: ask a doctor

+ 34 913456902 Monday to Friday: 9:00 am to 5:00 pm

  • keep the product in a cool and dry place

  • Apply a small amount the intimate parts and gently wash. Rinse with water
  • Maybe used as often as necessary

Water, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Disodium Laureth Sulfosuccinate, Lactic Acid, Diazolidinyl Urea, Glycyrrhizinic,Acid, Sodium Benzoate, Potassium Sorbate, Phytosphingosine HCl, Parfum

GLIZIGEN GEL INTIMATE 
glycerin gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64539-017
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
COCAMIDOPROPYL BETAINE12 mg  in 1 mL
GLYCYRRHIZIN0.1 mg  in 1 mL
POTASSIUM SORBATE0.1 mg  in 1 mL
SODIUM LAURYL SULFATE20 mg  in 1 mL
DISODIUM LAURETH SULFOSUCCINATE3 mg  in 1 mL
LACTIC ACID0.36 mg  in 1 mL
DIAZOLIDINYL UREA0.3 mg  in 1 mL
SODIUM BENZOATE0.1 mg  in 1 mL
PHYTOSPHINGOSINE0.01 mg  in 1 mL
WATER100 mg  in 1 mL
Packaging
#Item CodePackage Description
1NDC:64539-017-021 BLISTER PACK in 1 BOTTLE
1NDC:64539-017-01250 mL in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34703/18/2018
Labeler - Catalysis, SL (862795119)
Registrant - Catalysis, SL (862795119)
Establishment
NameAddressID/FEIOperations
Catalysis, SL862795119manufacture(64539-017)

 
Catalysis, SL

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.