Vaccine Information: Vaxchora (Page 4 of 4)

17 PATIENT COUNSELING INFORMATION

Prior to administration of this vaccine, the health care professional should inform the individual of the following:

Advise vaccine recipients to exercise caution regarding food and water consumed in cholera-affected areas, in accordance with the recommendations from the Centers for Disease Control and Prevention for the prevention of cholera in travelers.
Educate vaccine recipients regarding the most common adverse reactions occurring within 7 days post-vaccination with VAXCHORA (tiredness, headache, abdominal pain, nausea/vomiting, lack of appetite, and diarrhea).
Inform vaccine recipients that VAXCHORA is a live attenuated vaccine and has the potential for transmission of the vaccine strain to close contacts (e.g., household contacts). For at least 14 days following vaccination with VAXCHORA, vaccine recipients should wash their hands thoroughly after using the bathroom and before preparing or handling food.
Register women who receive VAXCHORA while pregnant in the pregnancy registry by calling 1-800-533-5899 [see Pregnancy (8.1)].
Instruct vaccine recipients to report adverse reactions to their healthcare provider.

VAXCHORA® is a registered trademark of PaxVax Bermuda Ltd.
US License No. 2041Manufactured by: PaxVax Bermuda Ltd.

Distributed by: PaxVax, Inc., 555 Twin Dolphin Drive, Suite 360, Redwood City, CA 94065, USA

© 2020 PaxVax. All rights reserved.

Artwork No. 1003808

PRINCIPAL DISPLAY PANEL — CARTON

Principal Display Panel -- Carton
(click image for full-size original)

Carton

NDC 70460-004-01

STORE REFRIGERATED
Use After Reconstitution

Cholera Vaccine, Live, Oral
Vaxchora®

Contents: Single-dose Active Packet (4×108 to 2×109 CFU of
Vibrio cholerae CVD 103-HgR) and Single-dose Buffer Packet.

Prior to administration, reconstitute Buffer in 100 mL of purified
bottled water or spring bottled water then add Active.
See package insert.

PaxVax

DISTRIBUTED BY: PaxVax, Inc.
555 Twin Dolphin Drive, Suite 360
Redwood City, CA 94065

Cholera Vaccine, Live, Oral
Vaxchora®

Live vaccine for oral, active immunization against cholera
Store at 36°F to 46°F (2°C to 8°C)

Administration and dosage: see package insert
US License No. 2041

Rx ONLY

GTIN:
S/N:
EXP:LOT:

PRINCIPAL DISPLAY PANEL — Active and Buffer Packets

Principal Display Panel -- Active and Buffer Packets
(click image for full-size original)

BUFFER COMPONENT
OF VAXCHORA®
(Cholera Vaccine, Live, Oral)

1

Packet 1 of 2. USE FIRST.

Contents (Single-Dose): Buffer

Directions: Add entire contents
of Packet 1 to 100 mL of purified
bottled or spring bottled water in
disposable cup, then stir. Go to
Packet 2. See package insert.

Rx Only — For Oral Administration

EXP: LOT:

NDC 70460-003-02

PaxVax Bermuda Ltd.
US License No. 2041

ACTIVE COMPONENT
of VAXCHORA®
(Cholera Vaccine, Live, Oral)

2

Packet 2 of 2. USE LAST.

Contents (Single-Dose):
4×108 to 2×109 CFU of
lyophilized Vibrio cholerae
CVD 103-HgR.

Direction: Add contents of Packet 2
to cup and stir to create vaccine. See
package insert.

Rx Only — For Oral Administration

EXP: LOT:

NDC 70460-002-02

PaxVax Bermuda Ltd.US License No. 2041 DSN104

VAXCHORA cholera vaccine, live, oral kit
Product Information
Product Type VACCINE Item Code (Source) NDC:70460-004
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70460-004-01 1 KIT in 1 CARTON None
Quantity of Parts
Part # Package Quantity Total Product Quantity
Part 1 1 PACKET 1
Part 2 1 PACKET 1
Part 1 of 2
VAXCHORA cholera vaccine, live, oral powder, for suspension
Product Information
Item Code (Source) NDC:70460-002
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN (VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN) VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN 1200000000 [CFU]
Inactive Ingredients
Ingredient Name Strength
SUCROSE
HYDROLYZED CASEIN (ENZYMATIC; 1000 MW)
ASCORBIC ACID
ANHYDROUS LACTOSE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70460-002-02 1 POWDER, FOR SUSPENSION in 1 PACKET None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA125597 09/15/2019
Part 2 of 2
BUFFER buffer powder, for suspension
Product Information
Item Code (Source) NDC:70460-003
Route of Administration ORAL DEA Schedule
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CARBONATE
ASCORBIC ACID
ANHYDROUS LACTOSE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70460-003-02 1 POWDER, FOR SUSPENSION in 1 PACKET None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA125597 02/13/2020
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA125597 02/13/2020
Labeler — Paxvax, Inc. (080128378)
Establishment
Name Address ID/FEI Operations
PaxVax Berna GmbH 480030654 API MANUFACTURE (70460-004), API MANUFACTURE (70460-002), API MANUFACTURE (70460-003), MANUFACTURE (70460-004), MANUFACTURE (70460-002), MANUFACTURE (70460-003), ANALYSIS (70460-004), ANALYSIS (70460-002), ANALYSIS (70460-003), PACK (70460-004), PACK (70460-002), PACK (70460-003)

Revised: 02/2020 Paxvax, Inc.

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