Label: DYNAREX HYDROGEL- glycerin gel
- NDC Code(s): 67777-233-01, 67777-233-02
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
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 November 29, 2022
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Warnings
- Dosage & Administration Dynarex Hydrogel
- Keep out of reach of children
- Indications and Usage:
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DYNAREX HYDROGEL
glycerin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-233 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 20 g in 100 g Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) EDETATE SODIUM (UNII: MP1J8420LU) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-233-02 24 in 1 CASE 05/26/2010 1 NDC:67777-233-01 84.7 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 05/26/2010 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)