GOODYS HEADACHE RELIEF SHOT- acetaminophen and caffeine liquid 
Medtech Products Inc.

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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Goodys Headache Relief Shot

Drug Facts

Active ingredients

(per 60 mL)

Acetaminophen 1000 mg

Caffeine 65 mg

Purpose

Pain reliever/ Pain Reliever Aid

Use

Temporarily relieves minor aches and pains due to:

•       headache

•       sore throat

•       minor arthritis pain

•       muscle aches

•       cold and flu

•       toothache

Warnings

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

you take

•       more than 4 Headache Relief Shots™ 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

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.

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

•       with any other drug containing acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

•       if you are allergic to acetaminophen or any of the inactive ingredients in this product      

Ask a doctor before use if

you have liver disease.      

Ask a doctor or pharmacist before use if

you are taking the blood thinning drug warfarin.      

Stop use and ask a doctor if

•       pain gets worse or lasts more than 10 days

•       fever gets worse or lasts more than 3 days

•       new symptoms occur

•       redness or swelling is present      

If pregnant or breastfeeding,

ask a healthcare professional before use.

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. Prompt medical attention is critical even if you do not notice any signs or symptoms.      

Directions

•       do not take more than directed (see overdose warning)

•       adults and children 12 years of age and over: take one Headache Relief Shot every 6 hours while symptoms persist; do not take more than 4 Headache Relief Shots in 24 hours.

•       children under 12 years of age: ask a doctor      

Other information

•       store at room temperature

•       read all product information before using      

Inactive ingredients

citric acid, flavor, glycerin, polyvinylpyrrolidone, potassium citrate, potassium sorbate, propylene glycol, purified water, sucralose      

Questions?

1-866-255-5197 GoodysHeadacheReliefShot.com




PRINCIPAL DISPLAY PANEL

NDC- 63029-639-01
Goody’s Headache Relief Shot
2 Pack
Berry

PRINCIPAL DISPLAY PANEL
NDC- 63029-639-01
Goody’s Headache Relief Shot
2 Pack 
Berry




PRINCIPAL DISPLAY PANEL

NDC- 63029-629-01
Goody’s Headache Relief Shot
2 Pack
Citrus

PRINCIPAL DISPLAY PANEL
NDC- 63029-629-01
Goody’s Headache Relief Shot
2 Pack 
Citrus




PRINCIPAL DISPLAY PANEL

NDC- 63029-629-02
Goody’s Headache Relief Shot
Single Dose

PRINCIPAL DISPLAY PANEL
NDC- 63029-629-02
Goody’s Headache Relief Shot
Single Dose

GOODYS HEADACHE RELIEF SHOT 
acetaminophen and caffeine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-639
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN1000 mg  in 60 mL
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE65 mg  in 60 mL
Inactive Ingredients
Ingredient NameStrength
POVIDONE K30 (UNII: U725QWY32X)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorCITRUSImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-639-012 in 1 DOSE PACK02/11/201306/30/2023
160 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product
2NDC:63029-639-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product02/11/201306/30/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34302/11/201306/30/2023
GOODYS HEADACHE RELIEF SHOT 
acetaminophen and caffeine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-629
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN1000 mg  in 60 mL
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE65 mg  in 60 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
POVIDONE K30 (UNII: U725QWY32X)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-629-012 in 1 DOSE PACK02/11/2013
160 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product
2NDC:63029-629-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product02/11/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34302/11/2013
Labeler - Medtech Products Inc. (122715688)

Revised: 6/2020
Document Id: c8b3641f-16a5-4677-b625-fef096440ffd
Set id: 374df462-aff6-4642-ba6f-e83a278fadcf
Version: 5
Effective Time: 20200626
 
Medtech Products Inc.