TOTALDRY SENSITIVE WASH- benzethonium chloride spray

TotalDry Sensitive Wash by

Drug Labeling and Warnings

TotalDry Sensitive Wash by is a Otc medication manufactured, distributed, or labeled by Secure Personal Care Products LLC, Westwood Laboratories LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzethonium Chloride 0.12%

Purpose

Antibacterial

Uses

TotalDry™ Sensitive Washis a delicate antibacterial
formulation for sensitive skin.

Warnings

For external use only.If rash or irritation develops,
discontinue use. Consult a physician if irritation persists.
Not for long-term use.​

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

Directions

Spray TotalDry™ Sensitive Washliberally on affected
area, then wipe clean.

Ingredients

Water, Propanediol, Aloe, Barbadensis (Aloe Vera) Leaf Juice,
Sodium Laureth Sulfate, Disodium Cocoamphodiacetate,
Polysorbate 80, PEG-12 - PEG-50 Lanolin, Lanolin Alcohol,
Phenoxyethanol, Ethylhexylglycerin, Citric Acid, Fragrance,
Yellow 10 (CI 47005)

Questions or Comments?

Please call 1-866-440-0049

Label

INGREDIENTS AND APPEARANCE

TOTALDRY SENSITIVE WASH 
benzethonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73703-124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.001212 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
ALOE (UNII: V5VD430YW9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PPG-12-PEG-50 LANOLIN (UNII: QJP3Q6598J)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73703-124-91	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/30/2025

Labeler - Secure Personal Care Products LLC (022013246)

Registrant - Westwood Laboratories LLC (832280635)

Establishment
Name	Address	ID/FEI	Business Operations
Westwood Laboratories LLC		832280635	pack(73703-124) , manufacture(73703-124) , label(73703-124)