DOC IN THE BOX ALL DAY SUPPLY- acetaminophen, calcium carbonate, dextromethorphan hbr, guaifenesin, phenylephrine hcl, ibuprofen, loperamide hcl 
Doc in the Box LLC

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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DOC IN THE BOX ALL DAY SUPPLY

EXTRA STRENGTH NON-ASPIRIN

Purpose

Pain reliever/fever reducer

EXTRA STRENGTH NON-ASPIRIN

Active ingredient (in each tablet)

Acetaminophen 500 mg

EXTRA STRENGTH NON-ASPIRIN

Uses

For the temporary relief of minor aches and pains associated with

For the reduction of fever.

EXTRA STRENGTH NON-ASPIRIN

Warnings
Liver warning:
This product contains acetaminophen. Severe liver damage may occur if you take:

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

EXTRA STRENGTH NON-ASPIRIN

Do not use

EXTRA STRENGTH NON-ASPIRIN

Ask a doctor before use if you have liver disease

EXTRA STRENGTH NON-ASPIRIN

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

EXTRA STRENGTH NON-ASPIRIN

Stop using and ask a doctor if

EXTRA STRENGTH NON-ASPIRIN

If pregnant or breast-feeding, ask a health professional before use.

EXTRA STRENGTH NON-ASPIRIN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

EXTRA STRENGH NON-ASPIRIN

Directions

Adults and children:

(12 years and older)

Take 2 tablets with water every 4 to 6 hours as needed.

Do not take more than 8 tablets in 24 hours.

Children under 12 years:

Do not give this adult strength product to children under

12 years of age; this will provide more than the recommended

dose (overdose) and may cause liver damage.

EXTRA STRENGTH NON-ASPIRIN

Other information


EXTRA STRENGTH NON-ASPIRIN

Inactive ingredients

corn starch, hypromellose, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone*, pregelatinized starch*, sodium starch glycolate*, stearic acid, titanium dioxide*.
* may contain

EXTRA STRENGTH NON-ASPIRIN

Questions? 1-800-634-7680

ANTACID

Active ingredient (in each tablet)

Calcium Carbonate 420 mg

ANTACID

Purpose

Antacid

ANTACID

Uses

For the relief of the following symptoms associated with

ANTACID

Warnings

ANTACID

Ask a doctor or health professional before use if you have

ANTACID

Stop using this product and ask a doctor if symptoms last more than 2 weeks

ANTACID

Do not exceed recommended dosage.

If pregnant or breast-feeding, ask a health professional before use.

ANTACID

Keep out of the reach of children.

ANTACID

Directions

ANTACID

Other information


ANTACID

Inactive ingredients

aspartame*, croscarmellose sodium*, gum acacia*, magnesium stearate, maltodextrin, mineral oil*, mint flavor, sorbitol*, sucrose*.
* may contain

ANTACID

Questions or comments? call 1-800-634-7680

COLD RELIEF

Active ingredient (in each tablet)

Acetaminophen 325 mg

Dextromethorphan Hydrobromide 15 mg

Guaifenesin 200 mg

Phenylephrine Hydrochloride 5 mg

COLD RELIEF

Purpose

Pain reliever/fever reducer

Cough suppressant

Expectorant

Nasal decongestant

COLD RELIEF

Uses

Temporarily relieves these cold symptoms

Temporarily reduces fever.

COLD RELIEF

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

COLD RELIEF

Do not use

COLD RELIEF

COLD RELIEF

Ask a doctor or pharmacist before use if you are

COLD RELIEF

When using this product

COLD RELIEF

Stop use and ask a doctor if

These could be signs of a serious condition.

COLD RELIEF

If pregnant or breast-feeding, ask a health professional before use.

COLD RELIEF

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

COLD RELIEF

Directions

Adults and children:

(12 years and older)

Take 2 tablets with water every 6-8 hours as needed. Do

not take more than 8 tablets in 24 hours.

Children under 12

years:

Do not give to children under 12 years of age.

COLD RELIEF

Other information

COLD RELIEF

Inactive ingredients maltodextrin, microcrystalline cellulose, povidone, sodium starch glycolate, starch, stearic acid

COLD RELIEF

Questions?

1-800-634-7680

IBUPROFEN

Active ingredient (in each tablet)

Ibuprofen 200 mg (NSAID)*

*non-steroidal anti-inflammatory drug

IBUPROFEN

Purpose

Pain reliever/fever reducer

IBUPROFEN

Uses

Temporarily relieves minor aches and pains associated with

Temporarily reduces fever.

IBUPROFEN

Warnings

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

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

Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

IBUPROFEN

Do not use

IBUPROFEN

Ask a doctor before use if

IBUPROFEN

Ask a doctor or pharmacist before use if you are

IBUPROFEN

When using this product

IBUPROFEN

Stop use and ask a doctor if

▪ feel faint ▪ vomit blood ▪ have bloody or black stools
▪ have stomach pain that does not get better

IBUPROFEN

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless specifically directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

IBUPROFEN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

IBUPROFEN

Directions

Adults and children:

(12 years and older)

Take 1 tablet every 4 to 6 hours while symptoms persist. If pain for fever

does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets

in 24 hours, unless directed by a doctor.

Children under 12 years:Do not give to children under 12 years of age.


IBUPROFEN

Other information


IBUPROFEN

Inactive ingredients

carnauba wax*, corn starch, hypromellose*, iron oxide red, lactose*, magnesium stearate*, microcrystalline cellulose*, polydextrose*, polyethylene glycol, polyvinyl alcohol*, povidone (K-30)*, silicon dioxide, sodium starch glycolate, stearic acid, talc*, titanium dioxide

* may contain

IBUPROFEN

Questions or comments?1-800-634-7680

DIAMODE

Active ingredient (in each caplet)

Loperamide Hydrochloride 2 mg

DIAMODE

Purpose

Antidiarrheal

DIAMODE

Uses

Controls the symptoms of diarrhea, including Traveler's diarrhea

DIAMODE

Warnings

Allergy alert: Do not use if you have ever had a rash or other allergic reaction to Loperamide HCl

DIAMODE

Do not use if you have bloody or black stool

DIAMODE

Ask a doctor before use if you have

DIAMODE

Ask a doctor or pharmacist before use if you are taking antibiotics

DIAMODE

When using this product

DIAMODE

Stop use and ask a doctor if

DIAMODE

If you are pregnant or breast-feeding, ask a health professional before use

DIAMODE

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIAMODE

Directions

Adults and children:

(12 years and older)

Take 2 caplets after the first loose stool

followed by 1 caplet after each subsequent

loose stool but no more than 4 caplets in 24 hours.

Children under 12 years:Do not give to children under 12 years of age.

DIAMODE

Other information

DIAMODE

Inactive ingredients anhydrous lactose, croscarmellose sodium, crospovidone, D&C Yellow #10, FD&C Blue #1, hydrogenated vegetable oil, magnesium stearate, powdered cellulose, pregelatinized starch

DIAMODE

Questions or comments? 1-800-634-7680

EXTRA STRENGTH NON-ASPIRIN

EXTRA STRENGTH

NON-ASPIRIN

2 Tablets

Mfd. for MEDIQUE PRODUCTS • Fort Myers, FL 33967

APAP image

ANTACID

ANTACID

2 Tablets

Mfd for MEDIQUE PRODUCTS, Fort Myers, FL 33967

Antacid

COLD RELIEF

COLD RELIEF

2 Tablets

Mfd for MEDIQUE PRODUCTS, Fort Myers, FL 33967

Cold Relief

IBUPROFEN

IBUPROFEN

2 Tablets

Mfd. for: MEDIQUE PRODUCTS Fort Myers, FL 33967

Ibuprofen

DIAMODE

Medique

Diamode

1 Caplet

Mfd. for MEDIQUE PRODUCTS, Fort Myers, FL 33967

Diamode

OUTER KIT CARTON

DOC IN THE BOX

ALL DAY SUPPLY...and More!

5 Different OTC Medications

17 Individual Packets

Headache, Toothache, Diarrhea, Cough/Cold, Upset Stomach, Heartburn, Muscle Aches

ALL PRODUCTS ARE PACKAGED IN TAMPER EVIDENT PACKETS. DO NOT USE IF ANY PACKETS ARE OPEN OR TORN.

KIT CONTENTSDrug Facts
Active ingredients (in each dosage unitPurposes
NON-ASPIRIN TABLETS (3 Packets, 2 Tablets Each)Acetaminophen 500 mgPain reliever/Fever reducer
ANTACID TABLETS (4 Packets, 2 Chewable Tablets Each)Calcium Carbonate 420 mgAntacid
COLD RELIEF TABLETS (3 Packets 2 Tablets Each)

Acetaminophen 325 mg

Dextromethorphan hydrobromide 15 mg

Guaifenesin 200 mg

Phenylephrine hydrochloride 5 mg

Pain reliever/Fever reducer

Cough suppressant

Expectorant

Nasal decongestant

IBUPROFEN TABLETS (3 Packets 2 Tablets Each)Ibuprofen 200 mg (NSAID)Pain reliever/Fever reducer
DIAMODE TABLETS (4Packets 1 Caplet Each)Loperamide hydrochloride 2 mgAntidiarrheal

SEE ENCLOSED PACKAGE INSERT FOR COMPLETE DRUG FACTS

Distributed by: DocintheBox, LLC, Florence, NJ 08518 • www.docinthebox.com

Carton Art Final

DOC IN THE BOX  ALL DAY SUPPLY
acetaminophen, calcium carbonate, dextromethorphan hbr, guaifenesin, phenylephrine hcl, ibuprofen, loperamide hcl kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72082-001
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72082-001-051 in 1 BOX; Type 1: Convenience Kit of Co-Package01/01/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 12 PACKET 3   in 2 
Part 22 PACKET 4   in 2 
Part 32 PACKET 3   in 2 
Part 42 PACKET 3   in 2 
Part 54 PACKET
Part 1 of 5
MEDI-FIRST NON-ASPIRIN EXTRA STRENGTH 
acetaminophen tablet, film coated
Product Information
Item Code (Source)NDC:47682-126
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE (UNII: FZ989GH94E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (Round) Size12mm
FlavorImprint Code FR;33
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-126-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34301/01/2019
Part 2 of 5
MEDI-FIRST ANTACID 
calcium carbonate tablet, chewable
Product Information
Item Code (Source)NDC:47682-820
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE420 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
ASPARTAME (UNII: Z0H242BBR1)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
ACACIA (UNII: 5C5403N26O)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SORBITOL (UNII: 506T60A25R)  
MINERAL OIL (UNII: T5L8T28FGP)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize11mm
FlavorImprint Code AZ;036
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-820-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33101/01/2019
Part 3 of 5
MEDI-FIRST COLD RELIEF 
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet
Product Information
Item Code (Source)NDC:47682-139
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg
Inactive Ingredients
Ingredient NameStrength
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (round) Size12mm
FlavorImprint Code FR;12
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-139-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34101/01/2019
Part 4 of 5
MEDI-FIRST IBUPROFEN 
ibuprofen tablet, coated
Product Information
Item Code (Source)NDC:47682-708
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POVIDONE K30 (UNII: U725QWY32X)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorred (Reddish brown) Scoreno score
ShapeROUNDSize10mm
FlavorImprint Code G;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-708-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07917401/01/2019
Part 5 of 5
MEDIQUE DIAMODE 
loperamide hydrochloride tablet
Product Information
Item Code (Source)NDC:47682-200
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE2 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
CROSPOVIDONE (UNII: 2S7830E561)  
CORN OIL (UNII: 8470G57WFM)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
Product Characteristics
ColorgreenScore2 pieces
ShapeOVALSize10mm
FlavorImprint Code 123
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-200-461 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07409101/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34301/01/2019
Labeler - Doc in the Box LLC (081033259)
Establishment
NameAddressID/FEIBusiness Operations
Doc in the Box LLC081033259repack(72082-001)

Revised: 1/2019
Document Id: 8526fa8e-4be1-eae7-e053-2a91aa0aa58e
Set id: 6545b440-21fe-fb21-e053-2991aa0a3e9f
Version: 5
Effective Time: 20190101
 
Doc in the Box LLC