2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE- aluminum chlorohydrate gel stick

Land: USA

Språk: engelska

Källa: NLM (National Library of Medicine)

Aktiva substanser:

ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)

Tillgänglig från:

American Consumer Products Corp

Administreringssätt:

TOPICAL

Receptbelagda typ:

OTC DRUG

Terapeutiska indikationer:

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.

Bemyndigande status:

OTC monograph final

Produktens egenskaper

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.
----------
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
aluminum chlorohydrate gel stick
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:72197-017
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE
- UNII:HPN8MZW13M)
ALUMINUM
CHLOROHYDRATE
20 g
in 100 g
American Consumer Products Corp
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ZINC PALMITATE (UNII: Q7407964JA)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
MINERAL OIL (UNII: T5L8T28FGP)
STEARIC ACID (UNII: 4ELV7Z65AP)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:72197-017-
02
64 g in 1 TUBE; Type 0: Not a Combination
Product
09/17/2019
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITAT