Meds on the Go

Manufacturer
Doc in the Box LLC
Effective date
2019-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:01

Label at a glance#

ProductMeds on the Go
Active ingredientACETAMINOPHEN, CALCIUM CARBONATE, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, IBUPROFEN, LOPERAMIDE HYDROCHLORIDE
Label structure77 sections

Storage and handling

Other information store at room temperature 59° - 86°F (15° - 30°C) tamper evident sealed packets do not use any opened or torn packets

Label contents#

Full prescribing information#

EXTRA STRENGTH NON-ASPIRIN

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)

Acetaminophen 500 mg

EXTRA STRENGTH NON-ASPIRIN

OTC - PURPOSE SECTION

Purpose

Pain reliever/fever reducer

EXTRA STRENGTH NON-ASPIRIN

INDICATIONS & USAGE SECTION

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.

EXTRA STRENGTH NON-ASPIRIN

WARNINGS SECTION

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

  • more than 8 tablets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

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

  • skin reddening
  • blisters
  • rash

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

EXTRA STRENGTH NON-ASPIRIN

OTC - DO NOT USE SECTION

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • for more than 10 days for pain unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor

EXTRA STRENGTH NON-ASPIRIN

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have liver disease

EXTRA STRENGTH NON-ASPIRIN

OTC - ASK DOCTOR/PHARMACIST SECTION

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

EXTRA STRENGTH NON-ASPIRIN

OTC - STOP USE SECTION

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

EXTRA STRENGTH NON-ASPIRIN

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

EXTRA STRENGTH NON-ASPIRIN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • ​do not use more than directed

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

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature 59° - 86°F (15° - 30°C)
  • tamper evident sealed packets
  • do not use any opened or torn packets

EXTRA STRENGTH NON-ASPIRIN

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions? 1-800-634-7680

ANTACID

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)

Calcium Carbonate 420 mg

ANTACID

OTC - PURPOSE SECTION

Purpose

Antacid

ANTACID

INDICATIONS & USAGE SECTION

Uses

For the relief of the following symptoms associated with

  • acid indigestion
  • sour stomach
  • heartburn
  • upset stomach

ANTACID

WARNINGS SECTION

Warnings

ANTACID

OTC - ASK DOCTOR SECTION

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

ANTACID

OTC - STOP USE SECTION

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

ANTACID

OTC - PREGNANCY OR BREAST FEEDING SECTION

Do not exceed recommended dosage.

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

ANTACID

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

ANTACID

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not use more than directed
  • Adults and children (12 years and older): Chew 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.

ANTACID

STORAGE AND HANDLING SECTION

Other information

  • Phenylketonurics: contains phenylalanine 1.5 mg per tablet
  • each tablet contains 168 mg of elemental calcium
  • store at room temperature 59° - 86°F (15° - 30°C)
  • tamper-evident sealed packets
  • do not use any opened or torn packets

ANTACID

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

ANTACID

OTC - QUESTIONS SECTION

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

COLD RELIEF

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)

Acetaminophen 325 mg

Dextromethorphan Hydrobromide 15 mg

Guaifenesin 200 mg

Phenylephrine Hydrochloride 5 mg

COLD RELIEF

OTC - PURPOSE SECTION

Purpose

Pain reliever/fever reducer

Cough suppressant

Expectorant

Nasal decongestant

COLD RELIEF

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves these cold symptoms

  • cough
  • sore throat
  • minor aches and pains
  • headache
  • nasal congestion
  • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Temporarily reduces fever.

COLD RELIEF

WARNINGS SECTION

Warnings

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

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

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

  • skin reddening
  • blisters
  • rash

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

OTC - DO NOT USE SECTION

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you have ever had an allergic reaction to this product or any of its ingredients
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

COLD RELIEF

OTC - ASK DOCTOR SECTION

  • liver disease
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • trouble urinating due to an enlarged prostate gland
  • cough that occurs with too much phlegm (mucus)
  • persistent or chronic cough that lasts as occurs with smoking, asthma, chronic bronchitis or emphysema

COLD RELIEF

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin

COLD RELIEF

OTC - WHEN USING SECTION

When using this product

  • do not use more than directed

COLD RELIEF

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • new symptoms occur
  • redness or swelling is present
  • pain or nasal congestion gets worse or lasts for more than 7 days
  • fever gets worse or lasts for more than 3 days
  • you get nervous, dizzy or sleepless
  • cough comes back or occurs with rash or headache that lasts.

These could be signs of a serious condition.

COLD RELIEF

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

COLD RELIEF

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature 59° - 86°F (15° - 30°C)
  • avoid excessive heat and humidity
  • tamper evident sealed packets
  • do not use any opened or torn packets

COLD RELIEF

INACTIVE INGREDIENT SECTION

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

COLD RELIEF

OTC - QUESTIONS SECTION

Questions?

1-800-634-7680

IBUPROFEN

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)

Ibuprofen 200 mg (NSAID)*

*non-steroidal anti-inflammatory drug

IBUPROFEN

OTC - PURPOSE SECTION

Purpose

Pain reliever/fever reducer

IBUPROFEN

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves minor aches and pains associated with

  • headache
  • toothache
  • backache
  • menstrual cramps
  • common cold
  • muscular aches
  • minor arthritis pain

Temporarily reduces fever.

IBUPROFEN

WARNINGS SECTION

Warnings

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

  • hives
  • skin reddening
  • asthma (wheezing)
  • facial swelling
  • rash
  • shock
  • blisters

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:

  • are age 60 or older
  • have had stomach ulcers or bleeding problems
  • taking a blood thinning (anticoagulant) or steroid drug
  • take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
  • have 3 or more alcoholic drinks every day while using this product
  • take more or for a longer time than directed

IBUPROFEN

OTC - DO NOT USE SECTION

Do not use

  • if you have ever had an allergic reaction to any other pain reliever/fever reducer
  • right before or after heart surgery

IBUPROFEN

OTC - ASK DOCTOR SECTION

Ask a doctor before use if

  • stomach bleeding warning applies to you
  • you have a history of stomach problems such as heartburn
  • you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
  • you are taking a diuretic
  • you have problems or serious side effects from taking pain relievers or fever reducers
  • you have asthma

IBUPROFEN

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

  • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
  • taking any other drug
  • under a doctor’s care for any serious condition

IBUPROFEN

OTC - WHEN USING SECTION

When using this product

  • the risk of heart attack or stroke may increase if you use more than directed or longer than directed
  • take with food or milk if stomach upset occurs

IBUPROFEN

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you experience any of the following signs of stomach bleeding

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

  • pain gets worse or lasts for more than 10 days
  • fever gets worse or lasts for more than 3 days
  • redness or swelling is present in the painful area
  • any new or unexpected symptoms occur

IBUPROFEN

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

IBUPROFEN

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not use more than directed
  • the smallest effective dose should be used
  • do not take longer than 10 days, unless directed by a doctor (see Warnings)

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

STORAGE AND HANDLING SECTION

Other information

  • read all product information before using
  • store at 68° - 77°F (20° - 25°C)
  • avoid excessive heat 104°F (above 40°C)
  • tamper evident sealed packets
  • do not use any opened or torn packet

IBUPROFEN

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions or comments?1-800-634-7680

DIAMODE

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each caplet)

Loperamide Hydrochloride 2 mg

DIAMODE

OTC - PURPOSE SECTION

Purpose

Antidiarrheal

DIAMODE

INDICATIONS & USAGE SECTION

Uses

Controls the symptoms of diarrhea, including Traveler's diarrhea

DIAMODE

WARNINGS SECTION

Warnings

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

DIAMODE

OTC - DO NOT USE SECTION

Do not use if you have bloody or black stool

DIAMODE

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a fever
  • mucus in stool
  • a history of liver disease

DIAMODE

OTC - ASK DOCTOR/PHARMACIST SECTION

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

DIAMODE

OTC - WHEN USING SECTION

When using this product

  • tiredness, drowsiness or dizziness may occur
  • be careful when driving or operating machinery

DIAMODE

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • symptoms get worse
  • diarrhea lasts more than 2 days
  • upi get abdominal swelling or bulging. These may be signs of a serious condition.

DIAMODE

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DIAMODE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIAMODE

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not use more than directed
  • drink plenty of clear fluids to help prevent dehydration caused by diarrhea

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

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature 68° - 77°F (20° - 25°C)
  • tamper-evident sealed packets
  • do not use any opened or torn packet

DIAMODE

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions or comments? 1-800-634-7680

EXTRA STRENGTH NON-ASPIRIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EXTRA STRENGTH

NON-ASPIRIN

2 Tablets

Mfd. for MEDIQUE PRODUCTS • Fort Myers, FL 33967

APAP imageAPAP image

ANTACID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTACID

2 Tablets

Mfd for MEDIQUE PRODUCTS, Fort Myers, FL 33967

AntacidAntacid

COLD RELIEF

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COLD RELIEF

2 Tablets

Mfd for MEDIQUE PRODUCTS, Fort Myers, FL 33967

Cold ReliefCold Relief

IBUPROFEN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IBUPROFEN

2 Tablets

Mfd. for: MEDIQUE PRODUCTS • Fort Myers, FL 33967

IbuprofenIbuprofen

DIAMODE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medique

Diamode

1 Caplet

Mfd. for MEDIQUE PRODUCTS, Fort Myers, FL 33967

DiamodeDiamode

OUTER CARTON PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDS ON THE GO...

INSTANT RELIEF ON THE GO!

5 Different OTC Medications

17 Individual Packets

HEADACHE, TOOTHACHE, MUSCLE ACHES, DIARRHEA, UPSET STOMACH, INDIGESTION, COUGH/COLD...AND MORE!

Acetaminophen • Ibuprofen • Anti-Diarrheal • Antacid • Decongestant

MEDSGO-PDPMEDSGO-PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1367204acetaminophen 325 MG / dextromethorphan HBr 15 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral TabletPSN1
198440acetaminophen 500 MG Oral TabletPSN1
313884calcium carbonate 420 MG (Ca 168 MG) Chewable TabletPSN1
978012Diamode 2 MG Oral TabletPSN1
310965ibuprofen 200 MG Oral TabletPSN1
978010loperamide HCl 2 MG Oral TabletPSN1
978012loperamide hydrochloride 2 MG Oral Tablet [Diamode]SBD1
1367204acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral TabletSCD1
198440acetaminophen 500 MG Oral TabletSCD1
313884calcium carbonate 420 MG Chewable TabletSCD1
310965ibuprofen 200 MG Oral TabletSCD1
978010loperamide hydrochloride 2 MG Oral TabletSCD1
1367204APAP 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral TabletSY1
198440APAP 500 MG Oral TabletSY1
313884calcium carbonate 420 MG (calcium 168 MG) Chewable TabletSY1
978012Diamode 2 MG Oral TabletSY1
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
GUAIFENESIN Pharmacologic Class Indexing1Indexing - Pharmacologic Class20211129
IBUPROFEN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20191108
LOPERAMIDE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
PHENYLEPHRINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
10f838ef-a72b-645d-80f8-e2255205c3b1Product name620240805
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814Product name320150910
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72082-002-052021-01-29C16284748780-1ba0f9c33-3012-a910-e053-dadaa90a0b85MEDS ON THE GO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-126-99Meds on the Go2 in 1 PACKETTABLET, FILM COATED3 in 2500 mg1
47682-139-99Meds on the Go2 in 1 PACKETTABLET3 in 25 mg1
47682-200-46Meds on the Go1 in 1 PACKETTABLET42 mg1
47682-708-99Meds on the Go2 in 1 PACKETTABLET, COATED3 in 2200 mg1
47682-820-99Meds on the Go2 in 1 PACKETTABLET, CHEWABLE4 in 2420 mg1
72082-002-05Meds on the Go1 in 1 BOXKIT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47682-126MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Legacy NDC20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip
47682-139MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Legacy NDC20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip
47682-200MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Current NDC, Legacy NDC20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip
47682-708MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Unmatched20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip
47682-820MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Current NDC, Legacy NDC20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip
72082-002MEDS ON THE GO (ACETAMINOPHEN, CALCIUM CARBONATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, IBUPROFEN, LOPERAMIDE HCL) KIT [DOC IN THE BOX LLC]1Legacy NDC, 6 package rows20190329_7db77515-9796-5094-e053-2a91aa0a0b9a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
47682-200-33EA - Each47682-200f07bc0d3-2ced-4052-ba14-126376ba97df12012-07-24
47682-200-50EA - Each47682-2001792fba4-32e7-461b-9844-385042675db512012-07-24
47682-200-64EA - Each47682-20094aca123-bb93-43e6-bf00-3c3df07db82a12023-08-08
47682-200-69EA - Each47682-20080247ac0-4431-4ac1-893d-7b7a9a0347e912012-07-24

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 53 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 56 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A074091-001LOPERAMIDE HYDROCHLORIDELOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1084e616aacf4f…
2026-08-18 06:07:402026-07A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1031067a03dcf5…
2025-08-23 18:47 UTC2025-08A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-106a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1003ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-102680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-105bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1079d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-101e350fbaab3a…
2024-05-31 18:47 UTC2024-05A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-108072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-105c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-105d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-104b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1074a2ff9319b5…
2022-03-09 01:35 UTC2022-03A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-1087673890dc5c…
2021-03-12 10:30 UTC2021-03A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-105aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-108869cabd3fbd…
2020-11-12 02:37 UTC2020-11A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10c0c555d07b60…
2019-12-14 00:12 UTC2019-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-103f01610625f2…
2019-09-15 20:21 UTC2019-09A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10b00525d2431f…
2019-07-19 19:46 UTC2019-07A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-106a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-101c564ffb4f44…
2023-12-20 04:57 UTC2023-12A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-109b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-103f0d92c62455…
2023-05-13 08:27 UTC2023-05A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10053a50430f4f…
2023-01-26 05:58 UTC2023-01A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-103bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-103a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A074091-001LOPERAMIDE HYDROCHLORIDE2MGTABLET / ORAL1992-12-10f41ea6bd6efb…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Private Label DistributorLOPERAMIDE HCL 2 MGUnifirst First Aid Corporation069e7979-a223-4819-b6cf-ea2731bf156b2025-12-01WarningsExact identifier
ndc (package): 47682-200-46
ndc (product): 47682-200
ndc11 (package): 47682020046
Medique AlcalakCALCIUM CARBONATEUnifirst First Aid Corporation60703e3d-52b1-49c4-b4e2-59d96fa09a782025-09-08WarningsExact identifier
ndc (package): 47682-820-99
ndc (product): 47682-820
ndc11 (package): 47682082099
7db77515-9797-5094-e053-2a91aa0a0b9a7db77515-9796-5094-e053-2a91aa0a0b9a2019-01-01WarningsExact identifier
spl id: 7db77515-9797-5094-e053-2a91aa0a0b9a
spl set id: 7db77515-9796-5094-e053-2a91aa0a0b9a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.