GANDH PROTECT ANTIPERSPIRANT DEODORANT ROLL ON- aluminum chlorohydrate gel

GandH Protect Antiperspirant Deodorant Roll On by

Drug Labeling and Warnings

GandH Protect Antiperspirant Deodorant Roll On by is a Otc medication manufactured, distributed, or labeled by Access Business Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Aluminum Chlorohydrate 25%

Purpose

Antiperspirant

Uses

Reduces underarm wetness.

Warnings

• For external use only.

Do not use

• on broken skin.

Stop use if

rash or irritation occurs.

Ask doctor before use

• if you have kidney disease.

Keep out of reach of children.

• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake before use. Apply to underarms only.

Inactive Ingredients:

Water, PPG-3 Myristyl Ether, Steareth-2, Steareth-20, Sodium Benzoate, Glycerin, Fragrance, Glycine, Allantoin, Caprylic/Capric Triglyceride, Lauric Acid, Propylene Glycol, Butylene Glycol, Bisabolol, Lecithin, Centella Asiatica Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Camellia Sinensis Leaf Extract, Myristic Acid, Phenoxyethanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Ceramide NP, Beta-Sitosterol, Chlorphenesin, Zingiber Officinale (Ginger) Root Extract, Tocopherol, Geraniol, Limonene, Linalool

Package Labeling:

INGREDIENTS AND APPEARANCE

GANDH PROTECT ANTIPERSPIRANT DEODORANT ROLL ON 
aluminum chlorohydrate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10056-534
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	250 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CHLORPHENESIN (UNII: I670DAL4SZ)
GINGER (UNII: C5529G5JPQ)
TOCOPHEROL (UNII: R0ZB2556P8)
GERANIOL (UNII: L837108USY)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
WATER (UNII: 059QF0KO0R)
PPG-3 MYRISTYL ETHER (UNII: 7913J43WZ5)
STEARETH-2 (UNII: V56DFE46J5)
STEARETH-20 (UNII: L0Q8IK9E08)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCINE (UNII: TE7660XO1C)
ALLANTOIN (UNII: 344S277G0Z)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
LAURIC ACID (UNII: 1160N9NU9U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
LEVOMENOL (UNII: 24WE03BX2T)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MYRISTIC ACID (UNII: 0I3V7S25AW)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ROSEMARY (UNII: IJ67X351P9)
CERAMIDE NP (UNII: 4370DF050B)
.BETA.-SITOSTEROL (UNII: S347WMO6M4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10056-534-00	1 in 1 BOX	03/12/2025
1		100 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	03/12/2025

Labeler - Access Business Group LLC (839830713)