NDC 64942-1260 Dove Go Fresh Restore Antiperspirant And Deodorant

Product Information

Product Packages

NDC 64942-1260-2

Package Description: 45 g in 1 CONTAINER

NDC 64942-1260-4

Package Description: 2 PACKAGE in 1 PACKAGE > 2 CONTAINER in 1 PACKAGE (64942-1260-3) > 74 g in 1 CONTAINER (64942-1260-1)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Dove Go Fresh Restore Antiperspirant And Deodorant is product labeled by Conopco Inc. D/b/a Unilever. The product's dosage form is and is administered via form.


What are Dove Go Fresh Restore Antiperspirant And Deodorant Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)


Inactive Ingredient(s)

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • STEARETH-100 (UNII: 4OH5W9UM87)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)


* Please review the disclaimer below.

Dove Go Fresh Restore Antiperspirant And Deodorant Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Otc - Active Ingredient



Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)


Otc - Purpose



Purpose
anti-perspirant


Indications & Usage



Uses· reduces underarm wetness   · 48 hour protection


Warnings



Warnings
For External Use Only


Otc - Do Not Use



Do not use on broken skin


Otc - Ask Doctor



Ask a doctor before use if you have kidney disease


Otc - Stop Use



Stop use if rash or irritation occurs


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.


Dosage & Administration



Directions  apply to underarms only


Inactive Ingredient



Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Fragrance (Parfum), Dimethicone,
Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT.


Otc - Questions



Questions?

Call toll-free 1-800-761-3683


Pdp 2.6 Oz.




2.6 Oz Twin Sleeve




* Please review the disclaimer below.