READY CARE XL KIT- first aid kit kit
Ready Care XL Kit by
Drug Labeling and Warnings
Ready Care XL Kit by is a Other medication manufactured, distributed, or labeled by Dukal Corporation. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- PRINCIPAL DISPLAY PANEL
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Back Label
Physicians Care
CLEANSE
20 Antiseptic Wipes
20 Alcohol PadsTREAT
6 Antibiotic Ointment Packets
PROTECT
6 Burn Ointment Packets
10 3" Cotton Tip Applicators3 Knuckle Bandages
3 Fingertip Bandages
35 3/8” x 1 1/2” Bandages
16 1” x 3” Bandages
200 3/4” x 3” Bandages
1 1/2" Tape
1 Triangular Bandage
4 3" x 3" Sterile Gauze Pads
1 Abdominal Compress
Medicine
3 Acetaminophen Packets (packet of 2)
3 Aspirin Packets (packets of 2)
3 Antacid Packets (packets of 2)
Other
Gloves (2 Pair)
1 Cold Pack
1 First Aid Guide
10 Finger Splints
5 Disposable Thermometers
1 Tweezer
Acme United Corporation
60 Round Hill Road
Fairfield CT 06824
www.acmeunited.com
Designed in the USA | Made in China
CAUTION: This product may contain natural rubber latex which may cause allergic reactions.
This kit contains products that have expiration dates. Please check before use.
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BZK Towelette Labeling
Reorder 855
NDC: 65517-0004-1
Dukal
BZK TOWELETTE
Contains Benzalkonium Chloride
For External Use Only
Helps Prevent Infection
1 / Pouch
DUKAL CORPORATION
(631) 656-3800
Ronkonkoma, NY 11779 www.dukal.com
Made in China
Drug Facts
Active Ingredients....................Benzalkonium Chloride 0.133% w/v
Purpose................................. First Aid Antiseptic
USE: Antiseptic Cleansing of face, hands and
body without soap and water. Airs dries in seconds
DO NOT USE: in the eyes or apply over large
areas of the body.
STOP USE: If irritation, redness or other symptoms
develop. Consult a doctor if the conditions persists
or gets worse.
CAUTION: Keep out of reach of children. If
swallowed get medical help or contact a Poison
Control Center right away.
DIRECTIONS: Tear open packet, unfold and use
as a washcloth.INACTIVE INGREDIENTS: Distilled Water
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Prep Pad Labeling
Reorder 852
Dukal Corporation
NDC: 65517-0001-1
NPN 80003156
ALCOHOL PREP PAD
Saturated with 70% Isopropyl Alcohol
For External Use Only
1 / Pouch
Dukal Corporation
Ronkonkoma, NY 11779
631-656-3800
www.dukal.com
Made in China
Drug Facts
Active Ingredients
Isopropyl Alcohol 70%
Purpose
Antiseptic Cleanser
Use
For Preparation of Skin prior to an injection
Warnings
- For External Use Only
- Flammable, Keep away from fire or flame
Do Not Use
- with electrocautery procedures
- In the Eyes. If contact occurs, flush eyes with water
Stop Use
If irritation and redness develop. If condition persists, consult your health care practitioner.Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.Directions
Wipe injection site vigorously and discard.Other Information
Store at Room Temperature 15 - 30 C (59 - 86 F)
Inactive Ingredient
purified water
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Triple Antibiotic Labeling
WaterJel
Triple Antibiotic
First Aid Ointment
To Help Prevent Infection
Each Gram contains
Bacitracin Zinc 400 units
Neomycin Sulphate 5 mg
(equivalent to 3.5 mg Neomycin base)
Polymyxin B Sulfate 5000 units
Water-Jel Technologies
Carlstadt, NJ 07072
Drug Facts
Uses to help prevent infection in
minor cuts, scrapes, burns
Warnings
For external use only
Do not use
in the eyes or apply over large areas of the body
If you are allergic to any of the ingredients
longer than 1 week unless directed by a doctor
Stop use and ask a doctor if
the condition persists or gets worse
a rash or other allergic reaction develops
Keep out of reach of children
if ingested contact Poison Control Center right away
Directions
clean affected area apply a small amount of product
(an amount equal to the surface area of the tip of a finger)
on the area 1 to 3 times daily may be covered with a sterile bandage
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First Aid Burn Cream Labeling
WaterJel
First Aid Burn Cream
Antiseptic Pain Relief with Aloe
Active Ingredients:
Benzalkonium Chloride 0.13%
Lidocaine HCL 0.5%
Water-Jel Technologies
Carlstadt, NJ 07072
Drug Facts
Purpose
First Aid Antiseptic, External analgesic
Uses
first aid to help prevent infection and for temporary
relief of pain an itching associated with minor cuts,
scrapes, burns
Warnings
For external use only
Do not use
in the eyes
in large quantities over raw or blistered areas or on
deep puncture wounds, animal bites, or serious burns
Keep out of reach of children
if ingested contact Poison Control Center right away
Directions
clean affected area apply a small amount not more
than 3 times daily may be covered with a sterile bandage
Other Information
Store at room temperature
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APAP Labeling
Drug Facts
Active Ingredients (In each tablet)...............Purposes
Acetaminophen 325 mg.............................Pain Reliever/Fever Reducer
Uses:
For the temporary relief of minor aches and pains associated with:
headache muscular aches minor arthritis pain
common cold toothache menstrual cramps
For the reduction of fever.
Warnings:
Alcohol Warning: If you consume 3 or more alcoholic drinks every day,
ask your doctor whether you should take acetaminophen or other pain
relievers/fever reducers. Acetaminophen may cause liver damage.
Do not use:
with any other product containing acetaminophen
for more than 10 days for pain unless directed by a doctor
for more than 3 days for fever unless directed by a doctor
Stop Using and Ask a Doctor If:
symptoms do not improve
new symptoms occur
pain or fever persists or gets worse
redness or swelling is present
Do not exceed recommended dosage. Keep this and all drugs out of the reach of children.
In case of accidental overdose, contact a physician or Poison Control Center immediately.
Prompt medical attention is critical for adults as well as for children even if you do not notice
any signs or symptoms.
If pregnant or breast feeding, ask a health professional before use.
Directions:
Do not use more than directed
Adults and children: (12 years and older)
Take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours,
or as directed by a doctor.
Children under 12 years:
Do not give to children under 12 years of age.
Other Information:
Store at room temperature
Tamper-Evident Sealed Packets
Do Not Use any Opened or Torn Packets
Inactive Ingredients:
Corn starch*, croscarmellose sodium, crospovidone, hypromellose, microcrystalline cellulose,
mineral oil, opadry clear, pharmaceutical glaze, polyethylene glycol, povidone*, pregelatinized
starch*, sodium carboxymethylcellulose, sodium starch glycolate, stearic acid*, talc*, titanium dioxide.
*may contain
Questions or comments? 1-800-634-7680
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Alcalak Labeling
Drug Facts
Active Ingredients (In each tablet)....................Purposes
Calcium Carbonate 420 mg ..............................Antacid
Uses:
For the relief of the following symptoms associated with:
acid indigestion sour stomach heartburn upset stomach
Warnings:
Ask a doctor or health professional before use if you have:
been taking a prescription drug. Antacids may interact with certain prescription drugs.
kidney stones
a calcium-restricted diet
Stop using this product and ask a doctor if:
symptoms last more than 2 weeks
Do not exceed recommended dosage.
Keep this and all drugs out of the reach of children. If you are pregnant or breast feeding,
ask a health professional before use.
Directions:
Do not use more than directed
Adults and children: (12 years and older)
Take 2 tablets every 2 or 3 hours as symptoms occur or as directed by a physician. Do not
take more than 19 tablets in a 24 hour period, or use the maximum dosage of this product for
more than 2 weeks, except under the advice and supervision of a physician.
Children under 12 years:
Do not give to children under 12 years of age.
Other Information:
Phenylketonurics: Contains Phenylalanine 1.5 mg per tablet
Each tablet contains 168 mg of elemental calcium
Store at room temperature in a dry place
Tamper-Evident Sealed Packets
Do not Use any Opened or Torn Packets
Inactive Ingredients:
aspartame*, carageenan*, croscarmellose sodium*, glycine*, magnesium stearate, mint flavor*,
silica*, sorbitol, spearmint flavor*, stearic acid*, stevix*, xylitol*
*may contain
Questions or comments? 1-800-634-7680 -
Aspirin Labeling
Drug Facts
Active Ingredients (In each tablet)..................Purposes
Aspirin 325mg (NSAID*) ...............................Pain Reliever / Fever Reducer
*nonsteroidal anti-inflammatory drug
Uses:
Temporarily relieves minor aches and pains due:
headache muscular aches minor arthritis pain backache
common cold toothache menstrual cramps
Temporarily reduces fever.
Warnings:
Reye's Syndrome: Children and teenagers should not use this medicine for chicken pox,
or flu symptoms before a doctor is consulted about Reye's Syndrome, a rare but serious
illness reported to be associated with aspirin.
Allergy Alert: Aspirin may cause a severe allergic reaction which may include:
hives skin reddening facial swelling rash asthma (wheezing) blisters shock
If an allergic reaction occurs, stop use and seek medical help right away.
Stomach Bleeding Warning: This product contains a nonsteroidal anti-inflammatory
drug (NSAID), which may cause stomach bleeding.
The chance is higher if you:
are age 60 or older have had stomach ulcers or bleeding problems
take a blood thinning (anticoagulant) or steroid drug
take other drugs containing an NSAID (aspirin, ibuprofen, naproxen, or others)
have 3 or more alcohol drinks every day while using this product
take more or for a longer time than directed
Do not use:
if you have ever had an allergic reaction to any other pain reliever/ fever reducer.
right before or after heart surgery
Ask a Doctor before use if you have:
problems or serious side effects from taking pain relievers or fever reducers
stomach problems that last or come back, such as heartburn, upset stomach, or
stomach pain ulcers bleeding problems high blood pressure
heart or kidney disease taken a diuretic reached age 60 or older
Ask a Doctor or Pharmacist before use if you are:
taking any other drug containing and NSAID (prescription or nonprescription)
taking a blood thinning (anticoagulant) or steroid drug
under a doctor’s care for any serious condition taking any other drug
When using this product:
take with food or milk if stomach upset occurs
long term continuous use may increase the risk of heart attack or stroke
Stop Using and Ask a Doctor If:
you feel faint, vomit blood, or have bloody or black stools. These are signs of
stomach bleeding. pain gets worse or lasts more than 10 days
fever gets worse or lasts more than 3 days you have difficulty swallowing
it feels like the pill is stuck in your throat you develop heartburn
stomach pain or upset gets worse or lasts
redness or swelling is present in the painful area any new symptoms appear
If pregnant or breast-feeding, ask a health professional before use. It is especially
important not to use aspirin during the last 3 months of pregnancy unless definitely
directed to do so by a doctor because it may cause problems in the unborn child or
complications during delivery.
Keep out of reach of children. In case of overdose, get medical help or contact a
Poison Control Center right away.
Directions:
Do not take more than directed.
The smallest effective dose should be used.
Do not take longer than 10 days, unless directed by a doctor (see Warnings)
Drink a full glass of water with each dose.
Adults and children: (12 years and older)
Take 1 or 2 tablets with water every 4 hours as needed. Do not take more than 12 tablets
in 24 hours, or as directed by a doctor.
Children under 12 years:
Do not give to children under 12 years of age.
Other Information:
Read all product information before using
Store at room temperature
Avoid excessive heat and humidity
Tamper evident sealed packets
Do not use any opened or torn packets
Inactive Ingredients:
Corn starch, croscarmellose sodium*, hypromellose*, microcrystalline cellulose*, mineral oil*,
polyethylene glycol, propylene glycol, silicon dioxide, starch, stearic acid, talc, titanium dioxide*.
*may contain
Questions or comments? 1-800-634-7680 - Ready Care XL Kit Label
- Ready Care XL Kit Back Label
- Prep Pad Labeling
- Antiseptic Towelette Label
- Antacid Label
- Acetaminophen Label
- Aspirin Label
- Triple Antibiotic Label
- Burn Cream Label
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INGREDIENTS AND APPEARANCE
READY CARE XL KIT
first aid kit kitProduct Information Product Type MEDICAL DEVICE Item Code (Source) NDC: 65517-0021 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 65517-0021-1 1 in 1 PACKAGE, COMBINATION Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 20 POUCH 8.0 mL Part 2 6 PACKET 5.4 g Part 3 6 PACKET 5.4 g Part 4 20 POUCH 28.0 mL Part 5 3 PACKET 6 Part 6 3 PACKET 6 Part 7 3 PACKET 6 Part 1 of 7 DUKAL ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Item Code (Source) NDC: 65517-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.70 mL in 1.0 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 65517-0001-1 0.4 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2000 Part 2 of 7 WATER-JEL 3-IN1 ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate and neomycin sulfate ointmentProduct Information Item Code (Source) NDC: 59898-740 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 59898-740-01 0.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 01/01/2010 Part 3 of 7 FIRST AID BURN
lidocaine hydrochloride and benzalkonium chloride creamProduct Information Item Code (Source) NDC: 59898-902 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) LIGHT MINERAL OIL (UNII: N6K5787QVP) STEARIC ACID (UNII: 4ELV7Z65AP) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) CETYL ALCOHOL (UNII: 936JST6JCN) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 59898-902-01 0.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 01/01/2010 Part 4 of 7 BZK TOWELETTE
benzalkonium chloride swabProduct Information Item Code (Source) NDC: 65517-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.00186 mL in 1.4 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 1.39814 mL in 1.4 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 65517-0004-1 1.4 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2006 Part 5 of 7 MEDIQUE APAP
acetaminophen tablet, film coatedProduct Information Item Code (Source) NDC: 47682-145 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSE (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 47682-145-99 2 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part343 12/30/2008 Part 6 of 7 MEDIQUE ASPIRIN
aspirin tablet, film coatedProduct Information Item Code (Source) NDC: 47682-116 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSE (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 10mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 47682-116-99 2 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part343 12/30/2008 Part 7 of 7 MEDIQUE ALCALAK
calcium carbonate tablet, chewableProduct Information Item Code (Source) NDC: 47682-088 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Calcium Carbonate (UNII: H0G9379FGK) (Calcium - UNII:SY7Q814VUP) Calcium Carbonate 420 mg Inactive Ingredients Ingredient Name Strength D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) SUCROSE (UNII: C151H8M554) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 12mm Flavor MINT (MINT) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 47682-088-99 2 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 12/30/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 05/01/2010 Labeler - Dukal Corporation (791014871)
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