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NDC 70533-0013-25 Harrys Extra Strength Antiperspirant Redwood 200 mg/g Details

Harrys Extra Strength Antiperspirant Redwood 200 mg/g

Harrys Extra Strength Antiperspirant Redwood is a TOPICAL STICK in the HUMAN OTC DRUG category. It is labeled and distributed by Harry's Inc.. The primary component is ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY.

Product Information

NDC	70533-0013
Product ID	70533-013_eb5468dd-59aa-dcd0-e053-2995a90a7193
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Harrys Extra Strength Antiperspirant Redwood
Proprietary Name Suffix	n/a
Non-Proprietary Name	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Product Type	HUMAN OTC DRUG
Dosage Form	STICK
Route	TOPICAL
Active Ingredient Strength	200
Active Ingredient Units	mg/g
Substance Name	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Labeler Name	Harry's Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	M019
Listing Certified Through	2024-12-31

Package

Package Images

NDC 70533-0013-25 (70533001325)

Pricing Information	N/A
NDC Package Code	70533-013-25
Billing NDC	70533001325
Package	70 g in 1 CONTAINER (70533-013-25)
Marketing Start Date	2022-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL adcd37de-a797-2b53-e053-2a95a90ac17b Details

Active Ingredient

ALUMINUM ZIRCONIIUM TRICHLOROHYDREX GLY 20%

Purpose

Antiperspirant

Use

Reduces underarm wetness.
Extra effective.

Warnings

For external use only

Do not use on broken skin

Ask doctor before use if you have kidney disease

Stop use if rash or irritation occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only
Apply at bedtime

Inactive Ingredients

STEARYL ALCOHOL, DIMETHICONE, C15-19 ALKANE, DIHEPTYL SUCCINATE, WATER/AQUA/EAU, C12-15 ALKYL BENZOATE, HYDROGENATED CASTOR OIL, CETYL ALCOHOL, SILICA, FRAGRANCE/PARFUM, ALUMINUM STARCH OCENTYLSUCCINATE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, ALLANTOIN, BISABOLOL, ZINGIBER OFFINCALE (GINGER) ROOT EXTRACT,

TOCOPHERYL ACETATE, MYRISTYL ALCOHOL, CITRONELLYL METHYLCROTONATE, CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, LIMONENE, LINALOOL, ALPHA-ISOMETHYL IONONE, BENZYL ALCOHOL, CITRAL, EUGENOL.

SPL UNCLASSIFIED SECTION

Questions?: 1-888-212-6855

PRINCIPAL DISPLAY PANEL

NDC: 70533-013-25

INGREDIENTS AND APPEARANCE

HARRYS EXTRA STRENGTH ANTIPERSPIRANT REDWOOD

aluminum zirconium trichlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70533-013
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	200 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
EUGENOL (UNII: 3T8H1794QW)
WATER (UNII: 059QF0KO0R)
C15-19 ALKANE (UNII: CI87N1IM01)
DIMETHICONE (UNII: 92RU3N3Y1O)
JOJOBA OIL (UNII: 724GKU717M)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
GINGER (UNII: C5529G5JPQ)
ALLANTOIN (UNII: 344S277G0Z)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
FRAGRANCE 13576 (UNII: 5EM498GW35)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
CITRONELLYL METHYLCROTONATE (UNII: K61O222P3D)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
CITRAL (UNII: T7EU0O9VPP)
CETYL ALCOHOL (UNII: 936JST6JCN)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Product Characteristics
Color	white (White Opaque Stick)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70533-013-25	70 g in 1 CONTAINER; Type 0: Not a Combination Product	05/01/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	M019	05/01/2022

Labeler - Harry's Inc. (079239206)

Revised: 5/2022

Document Id: eb5468dd-59aa-dcd0-e053-2995a90a7193

Set id: adcd37de-a797-2b53-e053-2a95a90ac17b

Version: 3

Effective Time: 20220501