OTC - ACTIVE INGREDIENT SECTION
Acetaminophen, Caffeine Anhydrous
Acetaminophen, Caffeine Anhydrous
relief of: Headaches, Aches, Pain and Fever
Keep out of reach of children
■ adult and children 12 years of age and older: 1 capsules three times a day
■ children under 12 years of age: ask a doctor
Do not use if carton is open or if printed bottle neck band or inner foil seal is broken.physician
Keep out of the reach of children. This package contains enough drug to seriously harm a child. Do not use with other drugs containing acetaminophen.
Use the smallest effective dose. Do not take more than the maximum daily dose. Overdose may result in severe or possibly fatal liver damage.
Do not take if allergic to acetaminophen. Consult a doctor if: your symptoms last for more than 5 days or fever lasts more than 3 days or you develop allergic reactions such as wheezing, rash or itching.
Ask a doctor or pharmacist before use if you: Are pregnant or breastfeeding, have chronic alcoholism; have a serious liver or kidney disease; use any other medications including natural health products, prescription drugs, salicylates or other pain and fever relief medications.
In case of overdose, call a Poison Control Centre or doctor immediately, even if you do not notice any possible signs or symptoms such as increased sweating, nausea, vomiting, stomach pain, and loss of appetite.
cellulose, corn starch, magnesium stearate, sodium starch glycolate
For oral use only
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| 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 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72689-0002-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4909-f424-e053-dadaa90a57ce | 7b0deef1-121d-4663-e053-2991aa0ab4b7 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72689-0002-1 | SARIDON - A | 10 in 1 BLISTER PACK | TABLET | 10 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72689-0002 | SARIDON - A (ACETAMINOPHEN) TABLET [OASIS TRADING] | 1 | Legacy NDC, 1 package rows | 20181120_7b0deef1-121d-4663-e053-2991aa0ab4b7.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72689-0002 | 72689-0002-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM STARCH GLYCOLATE TYPE A CORN | AG9B65PV6B | IACT |
| POWDERED CELLULOSE | SMD1X3XO9M | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| CAFFEINE | 3G6A5W338E | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 7b0dc2c6-8e97-c747-e053-2a91aa0afbf1 | 7b0deef1-121d-4663-e053-2991aa0ab4b7 | 2018-11-19 | Warnings | 7b0dc2c6-8e97-c747-e053-2a91aa0afbf1 7b0deef1-121d-4663-e053-2991aa0ab4b7 |
Adverse event summaries are temporarily unavailable. Other product information remains available.