Backprin
- Manufacturer
- HART Health
- Effective date
- 2020-06-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:16:24
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients (in each tablet):
Acetaminophen 250 mg
Caffeine 50 mg
Magnesium Salicylate (NSAID*) 290 mg (*nonsteroidal anti-inflammatory drug)
OTC - PURPOSE SECTION
Purpose:
Pain Reliever/Fever Reducer
Pain Reliever Aid
Pain Reliever/Fever Reducer
INDICATIONS & USAGE SECTION
Uses:
Temporarily relieves minor back pain
WARNINGS SECTION
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 salicylates.
Allergy alert: Acetaminophen and Magnesium Salicylate may cause severe allergic reaction which may include hives, skin reddening, blisters, rash, facial swelling, asthma (wheezing), or shock.
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
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is highter if you:
- take more or for a longer time than directed
- are age 60 or older
- have had stomach ulcers or bleeding problems
- take a blood thinning (anticoagulant) or steroid drug
- have 3 or more alcoholic drinks every day while using this product
- take other drugs containing prescription or non-prescription NSAID (aspirin, ibuprofen, naproxen, others)
OTC - DO NOT USE SECTION
Do not use:
- if you have ever had an allergic reaction to any other pain reliever/fever reducer
- with any other drug containing acetaminophen (prescription or non-prescription)
OTC - ASK DOCTOR SECTION
Ask a doctor before use if
- you have asthma, high blood pressure, heart disease, liver cirrhosis, or kidney disease
- stomach bleeding warning applies to you
- you are taking a diuretic
- you have a history of stomach problems, such as heartburn
Ask a doctor or pharmacist before use if you
- take a blood thinning (anticoagulant) or steroid drug
- take any drug for diabetes, gout or arthritis
- do not know if other drugs you are taking contain acetaminophen
- take any other drug containing an NSAID
OTC - STOP USE SECTION
Stop use and ask a doctor if:
- an allergic reaction occurs, seek medical help right away
- fever worsens or lasts for more than 3 days
- redness or swelling is present
- new symptoms occur
- pain worsens or lasts for more than 10 days
- ringing in the ears or a loss of hearing occurs
- you have any of the following signs of stomach bleeding: feel faint, vomit blood, have bloods or black stools, or stomach pain that does not get better
These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use salicylates 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.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OVERDOSAGE SECTION
Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symtoms. In case of overdose, get medical help or contact a Poison Control Center right away. 1-800-222-1222
DOSAGE & ADMINISTRATION SECTION
Directions:
Do not take more than directed
Adults and children 12 years of age and over:
- take 2 tablets with water every 4 hours while symptoms persist.
- do not take more than 8 tablets in 24 hours unless directed by a doctor
Children under 12 years of age: ask a doctor
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Hypromellose, Maltodextrin, Microcystalline Cellulose, Povidone, Polyethylene Glycol, Starch, Stearic Acid, Titanium Dioxide
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 283274 | acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet | PSN | 2 |
| 884770 | BACKPRIN 250 MG / 50 MG / 290 MG Oral Tablet | PSN | 2 |
| 884770 | acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet [Backprin] | SBD | 2 |
| 283274 | acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet | SCD | 2 |
| 283274 | APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral Tablet | SY | 2 |
| 884770 | APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral Tablet [Backprin] | SY | 2 |
| 884770 | Backprin (acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG) Oral Tablet | SY | 2 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7dea7767-9f52-b60a-5435-33cb9cc28bae | Product name | 4 | 20250124 |
| 6338270f-96cb-0ecb-6fbb-0a9bc78001f4 | Product name | 7 | 20250116 |
| 0ca83774-3f79-b837-5d6f-c210102f3bc8 | Product name | 6 | 20250114 |
| 41b814f3-0166-1c53-c9ef-a0794c7daf9d | Product name | 3 | 20221110 |
| a590be26-846c-8659-a5a1-fb25907965dc | Product name | 2 | 20221110 |
| 2dc76302-91c0-4c35-ad78-99adfb049c4b | Product name | 1 | 20200603 |
| e6065d4b-5ae1-476f-a40e-f2851cbb5d2b | Product name | 2 | 20180221 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 332e86c3-7875-ca6e-f934-2206d2b31996 | Product name | 1 | 20140508 |
| 56625fcc-aa34-9d30-d0e9-1c1beb37ea21 | Product name | 1 | 20140508 |
| 7dfac40f-a405-cd2e-7c06-3059ec0e1092 | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
| d223c173-c39b-d764-47d4-d671d3088815 | Product name | 1 | 20140508 |
| e01133ad-4dcd-c7f3-454b-2ff569ee160a | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50332-0116-2 | 2022-01-28 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
| 50332-0116-4 | 2022-01-28 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
| 50332-0116-2 | 2021-11-22 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
| 50332-0116-4 | 2021-11-22 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
| 50332-0116-2 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
| 50332-0116-4 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-1f44-fd44-e053-dadaa90aa01b | BACKPRIN |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50332-0116 | BACKPRIN (ACETAMINOPHEN, CAFFEINE, SALICYLAMIDE) TABLET [HART HEALTH] | 2 | Legacy NDC | 20200607_a9301898-2c72-4ec0-bba1-1a2eb1962a38.zip |
Products#
Every source-derived product name is available through these pages.
- Backprin
- Acetaminophen, caffeine, salicylamide
- ACETAMINOPHEN
- CAFFEINE
- MAGNESIUM SALICYLATE
- SALICYLIC ACID
- MALTODEXTRIN
- MICROCRYSTALLINE CELLULOSE
- POVIDONE
- STEARIC ACID
- TITANIUM DIOXIDE
- HYPROMELLOSES
- STARCH, CORN
- POLYETHYLENE GLYCOL, UNSPECIFIED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50332-0116 | 50332-0116-4, 50332-0116-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| CAFFEINE | 3G6A5W338E | ACTIB |
| MAGNESIUM SALICYLATE | 41728CY7UX | ACTIB |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POVIDONE | FZ989GH94E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5963362c-d180-49bd-be56-f2776ac7e746 | a9301898-2c72-4ec0-bba1-1a2eb1962a38 | 2020-06-05 | Warnings | 5963362c-d180-49bd-be56-f2776ac7e746 a9301898-2c72-4ec0-bba1-1a2eb1962a38 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
