BETASEPT- antiseptic surgical scrub solution 
Atlantis Consumer Healthcare, Inc.

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BETASEPT Antiseptic Surgical Scrub

Chlorhexidine Gluconate 4%

Drug Facts
Active ingredient Purpose
Chlorhexidine gluconate 4% solution

Purpose
Antiseptic

Uses

Warnings
For external use only
Allergy alert:
This product may cause a severe allergic reaction. Symptoms may include:

If an allergic reaction occurs, stop use and seek medical help right away.

Do not use

When using this product

Stop use and ask a doctor if irritation,sensitization, or allergic reaction occurs. These may be signs ofa serious condition.

Keep out of reach of children. Ifswallowed, get medical help or contact a Poison Control Center rightaway.

Directions

Surgical hand scrub:

Healthcare personnelhandwash:

Skin wound and general skin cleansing:

Other information

Inactive ingredients cocamide DEA, fragrance, glucono-delta-lactone, hydroxyethylcellulose, isopropyl alcohol, lauramine oxide, PEG-75 lanolin, purified water, tridecyl alcohol

Questions or comments? call 1-888-827-0624 (8am-5pm, EST, Mon-Fri.)

WARNING: This product can expose you to chemicals including coconut oil diethanolamine condensate (cocamide diethanolamine), which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov

Dist. by: Avrio Health L.P. Stamford, CT 06901-3431

304978-0A

BETASEPT
Antiseptic Surgical Scrub
NDC: 67618–200–30

304978-0A
BETASEPT 
antiseptic surgical scrub solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67618-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Chlorhexidine Gluconate (UNII: MOR84MUD8E) (Chlorhexidine - UNII:R4KO0DY52L) Chlorhexidine Gluconate.04 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
WATER (UNII: 059QF0KO0R)  
TRIDECYL ALCOHOL (UNII: 8I9428H868)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67618-200-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/1993
2NDC:67618-200-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/1993
3NDC:67618-200-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/1993
4NDC:67618-200-30946 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/1993
5NDC:67618-200-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/199301/31/2023
6NDC:67618-200-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/199305/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01912506/01/1993
Labeler - Atlantis Consumer Healthcare, Inc. (118983925)
Registrant - Atlantis Consumer Healthcare, Inc. (118983925)

Revised: 12/2023
Document Id: 38dcb5ed-dbcd-42dd-9851-23061fed37b1
Set id: 7e64e7bf-e88f-4056-c9e1-b49a277daa6c
Version: 10
Effective Time: 20231222
 
Atlantis Consumer Healthcare, Inc.