SOFT AND DRI CLINICAL EVERFRESH BLOSSOM- aluminum chlorohydrate aerosol, spray 
Golden Sun Inc DBA Newhall Laboratories

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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SOFT & DRI® Clinical Aerosol Everfresh Blossom

Drug Facts

Active ingredient

Aluminum Chlorohydrate 20%

Purpose

Antiperspirant

Use

reduces underarm perspiration

Warnings

For external use only

Flammable

  • do not spray near flame or while smoking
  • contents under pressure; do not crush, puncture, or incinerate
  • do not store at temperatures above 120° F

Do not use on broken skin

Ask a doctor before use if

you have kidney disease

Stop use and ask a doctor if

rash or irritation occurs

When using this product

  • use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal
  • avoid spraying in eyes
  • keep away from face and mouth to avoid breathing it

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away

Directions

Shake well. Apply to underarms only.

Inactive ingredients

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Cyclotetrasiloxane, Talc, Silica Dimethyl Silylate, Fragrance (Parfum), Silica

For questions or the latest product news, visit www.softndri.com

DISTRIBUTED BY
Newhall Laboratories
5 High Ridge Park
Stamford, CT 06905

PRINCIPAL DISPLAY PANEL - 170 g Can Label

SOFT
&DRI®

aerosol

KEEPS YOU FRESH AND DRY
FOR 24 HOURS

Soft Scent

ANTIPERSPIRANT DEODORANT

NET WT 6.0 OZ (170 g)

PRINCIPAL DISPLAY PANEL - 170 g Can Label
SOFT AND DRI CLINICAL EVERFRESH BLOSSOM 
aluminum chlorohydrate aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:31774-1046
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Chlorohydrate (UNII: HPN8MZW13M) (Aluminum Chlorohydrate - UNII:HPN8MZW13M) Aluminum Chlorohydrate200 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Butane (UNII: 6LV4FOR43R)  
1,1-Difluoroethane (UNII: 0B1U8K2ME0)  
Cyclomethicone 5 (UNII: 0THT5PCI0R)  
Cyclomethicone 4 (UNII: CZ227117JE)  
Talc (UNII: 7SEV7J4R1U)  
Silica Dimethyl Silylate (UNII: EU2PSP0G0W)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:31774-1046-1170 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/02/2014
Labeler - Golden Sun Inc DBA Newhall Laboratories (060383791)

Revised: 11/2015
Document Id: 0440e0d1-c66c-4b04-a6f3-df5d377ee434
Set id: d9aaa388-27c7-4143-93a3-ea6c682a93d8
Version: 1
Effective Time: 20151105
 
Golden Sun Inc DBA Newhall Laboratories