Himmy Pet BathWipe (Lavender Bliss)

Himmy Pet BathWipe by

Drug Labeling and Warnings

Himmy Pet BathWipe by is a Otc medication manufactured, distributed, or labeled by Ningbo Riway Daily Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HIMMY PET BATHWIPE- benzalkonium chloride cloth 
Ningbo Riway Industrial Co., Ltd.

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Himmy Pet BathWipe (Lavender Bliss)

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 0.10%

Purpose

Antiseptic

Use

For pet cleaning.

Warnings

For external use only.

Do not use

Do not use in eyes.In case of contact,rinse thoroughly with water.

Stop use and ask doctor if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a Poison Control Center.

Directions

Open the bag from the tear opening and use.

Thoroughly wipe pets, allow to dry without rinsing.

Discard after single use.

Other information

Do not flush down toilet.

Keep away from sunlight.Store at room temperature 20°-25° Celsius(68°-77° Fahrenheit).

May discolor certain fabrics.

Use within 2 weeks of opening.

Inactive ingredients

Aqua, Polysorbate 20, Decyl glucoside, Aloe Barbadensis Leaf Extract, Cetylpyridinium Chloride, Phenoxyethanol, Citric Acid, Disodium EDTA, Propylene Glycol, Sodium Hypochlorite, Witch Hazel Extract, Fragrance Lavender Bliss.

Himmy Pet BathWipe (Lavender Bliss) Package Label

49 g in 1 Bag(1 Wipe),NDC: 77267-011-01

HIMMY PET BATHWIPE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77267-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WITCH HAZEL (UNII: 101I4J0U34)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALOE (UNII: V5VD430YW9)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77267-011-01	3 in 1 BOX	12/08/2022	12/31/2023
1		49 g in 1 BAG; Type 0: Not a Combination Product
2	NDC: 77267-011-02	3 in 1 BOX	12/08/2022	12/31/2023
2		123 g in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/08/2022	12/31/2023

Labeler - Ningbo Riway Industrial Co., Ltd. (540997562)

Registrant - Ningbo Riway Industrial Co., Ltd. (540997562)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Riway Industrial Co., Ltd.		540997562	manufacture(77267-011)

Revised: 12/2025

Document Id: 47280481-fa40-77e7-e063-6294a90a8386

34390-5

Set id: ef493f84-ba6e-c46e-e053-2995a90aca7a

Version: 3

Effective Time: 20251230