EverDry 2.5 OZ Anti Perspirant Invisible Solid

EverDry 2.5 OZ Anti Perspirant Invisible Solid

Drug Labeling and Warnings

Drug Details

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2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE- aluminum chlorohydrate gel stick 
American Consumer Products Corp

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.

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EverDry 2.5 OZ Anti Perspirant Invisible Solid

Active ingredients: Aluminum Chlorohydrate 20%

Purpose: Antiperspirant

Warnings: For external use only.

Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

Ingredients: Mineral Oil, Stearic Acid, Stearyl Alcohol, Zinc, Palmitate, Cyclopentasiloxane, Hydrogenated Castor Oil, Fragrance, Silica, PPG-14 Butyl Ether, PEG-8 Disterate, BHT.

Directions: Twist base. Smooth onto dry underarms. Apply to underarms only.

Use: reduces underarm wetness and perspiration.

Stop use and ask a doctor if irritation or rash develops.

Do not use on broken or irritated skin.

EverDry Anti Perspirant Invisible

2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE 
aluminum chlorohydrate gel stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72197-017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
LAURYL PALMITATE (UNII: X3V3247O54)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ZINC (UNII: J41CSQ7QDS)  
TALC (UNII: 7SEV7J4R1U)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72197-017-0264 g in 1 TUBE; Type 0: Not a Combination Product09/17/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35009/17/2019
Labeler - American Consumer Products Corp (081101181)

Revised: 9/2019
 
American Consumer Products Corp


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