STANBACK- aspirin and caffeine powder 
Medtech Products Inc.

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Stanback

Drug Facts

Active ingredient

(in each powder)

Aspirin (NSAID*) 845 mg

*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

Active ingredient

(in each powder)

Caffeine 65 mg

Purpose

Pain reliever aid

Uses

Warnings

Reye’s syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye’s syndrome, a rare but serious illness.

Allergy alert: Aspirin may cause a severe allergic reaction which may include:

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

Caffeine Warning: This product contains caffeine. Limit the use of caffeine-containing medications,foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and , occasionally, rapid heart beat.

Do not use

if you have ever had an allergic reaction to aspirin or any other pain reliever/fever reducer

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 asthma

Ask a doctor or pharmacist before use if you are

taking a prescription drug for

  • diabetes
  • gout
  • arthritis

Stop use and ask a doctor if

  • an allergic reaction occurs. Seek medical help right away.
  • 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 more than 10 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • any new symptoms appear
  • ringing in the ears or a loss of hearing occurs

These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health care 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 (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

docusate sodium, fumaric acid, lactose monohydrate, potassium chloride

Questions?

1-866-255-5197 






PRINCIPAL DISPLAY PANEL

STANBACK

ASPIRIN (NSAID) - PAIN RELIEVER

CAFFEINE - PAIN RELIEVER AID


50 POWDERS

PRINCIPAL DISPLAY PANEL
STANBACK
ASPIRIN (NSAID) - PAIN RELIEVER 
CAFFEINE - PAIN RELIEVER AID

50 POWDERS

STANBACK 
aspirin and caffeine powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-501
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE65 mg
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN845 mg
Inactive Ingredients
Ingredient NameStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
FUMARIC ACID (UNII: 88XHZ13131)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-501-0150 in 1 CARTON; Type 0: Not a Combination Product10/01/2012
2NDC:63029-501-2424 in 1 CARTON; Type 0: Not a Combination Product10/01/201211/20/2023
3NDC:63029-501-022 in 1 PACKAGE; Type 0: Not a Combination Product10/01/2012
4NDC:63029-501-066 in 1 PACKAGE; Type 0: Not a Combination Product10/01/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01310/01/2012
Labeler - Medtech Products Inc. (122715688)

Revised: 1/2025
Document Id: c7af9f6c-018c-4612-b0a6-ba2e90fbec37
Set id: caaa1313-09e4-45aa-8836-346f6a370196
Version: 12
Effective Time: 20250117
 
Medtech Products Inc.