2.25OZ EVERDRY ULTRA DRY ANTIPERSPIRANT- aluminum chlorohydrate gel stick

United States - English - NLM (National Library of Medicine)

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Active ingredient:
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)
Available from:
American Consumer Products Corp
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
Purpose: Antiperspirant 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.
Authorization status:
OTC monograph final
Authorization number:
72197-018-02

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.

2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE

American Consumer Products Corp

aluminum chlorohydrate gel stick

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:7219 7-0 17

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ALUMINUM CHLO RO HYDRATE (UNII: HPN8 MZW13M) (ALUMINUM CHLOROHYDRATE -

UNII:HPN8 MZW13M)

ALUMINUM

CHLOROHYDRATE

20 g

in 10 0 g

Inactive Ingredients

Ingredient Name

Stre ng th

PPG-14 BUTYL ETHER (UNII: R19 9 TJT9 5T)

MINERAL O IL (UNII: T5L8 T28 FGP)

STEARIC ACID (UNII: 4ELV7Z6 5AP)

STEARYL ALCO HO L (UNII: 2KR8 9 I4H1Y)

LAURYL PALMITATE (UNII: X3V3247O54)

CYCLO METHICO NE 5 (UNII: 0 THT5PCI0 R)

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4)

PEG-8 DISTEARATE (UNII: 7JNC8 VN0 7M)

BUTYLATED HYDRO XYTO LUENE (UNII: 1P9 D0 Z171K)

ZINC (UNII: J41CSQ7QDS)

TALC (UNII: 7SEV7J4R1U)

HYDRO GENATED CASTO R O IL (UNII: ZF9 4AP8 MEY)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:7219 7-0 17-0 2

6 4 g in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct

0 9 /17/20 19

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph final

pa rt350

0 9 /17/20 19

Labeler -

American Consumer Products Corp (081101181)

Revised: 9/2019

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