SOFT AND DRI CLINICAL EVERFRESH BLOSSOM- aluminum chlorohydrate aerosol, spray

SOFT and DRI Clinical Everfresh Blossom by

Drug Labeling and Warnings

SOFT and DRI Clinical Everfresh Blossom by is a Otc medication manufactured, distributed, or labeled by Golden Sun Inc DBA Newhall Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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

QUESTIONS

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

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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)

INGREDIENTS AND APPEARANCE

SOFT AND DRI CLINICAL EVERFRESH BLOSSOM 
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 31774-1046
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Aluminum Chlorohydrate (UNII: HPN8MZW13M) (Aluminum Chlorohydrate - UNII:HPN8MZW13M)	Aluminum Chlorohydrate	200 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 31774-1046-1	170 g in 1 CAN; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/02/2014

Labeler - Golden Sun Inc DBA Newhall Laboratories (060383791)