Puricia Sanitizing Wipes (Blossom)

Puricia Sanitizing Wipes ( Blossom) by

Drug Labeling and Warnings

Puricia Sanitizing Wipes ( Blossom) by is a Otc medication manufactured, distributed, or labeled by PHARMABERG INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURICIA SANITIZING WIPES ( BLOSSOM)- ethyl alcohol, benzalkonium chloride, cetylpyridinium chloride,didecyl dimethyl ammonium chloride, chlorphenesin, phenoxyethanol cloth 
PHARMABERG INC.

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.

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Puricia Sanitizing Wipes (Blossom)

The Puricia Sanitizing Wipes are the easiest and the most convenient way to clean. The wipe's tough texture cleans and kills 99% of germs.

DIRECTIONS FOR USE:

(Bag)
1. Open the flip.
2. Pull out wipes one by one & use.
3. Please reseal after use to prevent moisture loss.

(Canister)
1. Open the lid of the container. Tear open the foil
2. Thread first sheet in CENTER of roll through slits in lid. Replace lid.
3. Pull out wipes one by one & use. Please reseal after use to prevent moisture loss.

STORAGE:

Keep the bags tightly closed in a dry, cool and well-ventilated place. Recommended storage temperature: 0°C to 40°C.

Active ingredients

Ethyl alcohol 65%
Benzalkonium Chloride 0.13%
Cetylpyridinium Chloride 0.05%
Didecyl Dimethyl Ammonium Chloride 0.10%
Chlorophenesin 0.05%
Phenoxyethanol 0.30%

Purpose

Antiseptic

Uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use. Do not push fingers through opening.

Warnings

For external use only: Hands. Do not use in the eyes.

keep out of reach of children and pets except with adult supervision.

Read product label carefully before use.If you have a hypersensitivity to any of the components of the formula, do not use the product.

In case of eye contact ,rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center right away.

Keep wipes inside original packaging. Store unopened packages in a cool, dry place away from direct light inaccessible to small children.
After use, dispose the wipes in the trash. DO NOT flush in toilet.

Inactive ingredients

Water, Citric Acid, Glycerol, Propylene Glycol, Matricaria recutita and Scent (Blossom)

Recommended for repeated use.

Puricia Sanitizing Wipes (50/Bag) / Blossom

NDC : 77302-005-01

Puricia Sanitizing Wipes (80/ Canister) / Blossom / English label

NDC : 77302-005-02

Puricia Sanitizing Wipes (80/ Canister) / Blossom / French label

NDC : 77302-005-02

PURICIA SANITIZING WIPES ( BLOSSOM) 
ethyl alcohol, benzalkonium chloride, cetylpyridinium chloride,didecyl dimethyl ammonium chloride, chlorphenesin, phenoxyethanol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77302-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.1 U  in 100 U
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 U  in 100 U
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 U  in 100 U
PHENOXYETHANOL (UNII: HIE492ZZ3T) (PHENOXYETHANOL - UNII:HIE492ZZ3T)	PHENOXYETHANOL	0.3 U  in 100 U
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	0.05 U  in 100 U
CHLORPHENESIN (UNII: I670DAL4SZ) (CHLORPHENESIN - UNII:I670DAL4SZ)	CHLORPHENESIN	0.05 U  in 100 U

Inactive Ingredients
Ingredient Name	Strength
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77302-005-01	50 U in 1 BAG; Type 0: Not a Combination Product	11/03/2020
2	NDC: 77302-005-02	80 U in 1 CANISTER; Type 0: Not a Combination Product	11/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/03/2020	06/01/2021

Labeler - PHARMABERG INC. (204355565)

Revised: 8/2021

Document Id: cad00412-4b53-754a-e053-2a95a90a3411

34390-5

Set id: b32c9cd5-6345-8b8e-e053-2995a90aeb91

Version: 2

Effective Time: 20210830