NOBLEAID PAIN RELIEVER- aspirin tablet, delayed release

NobleAid PAIN RELIEVER by

Drug Labeling and Warnings

NobleAid PAIN RELIEVER by is a Otc medication manufactured, distributed, or labeled by Noble Otc LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient (in each tablet)

Aspirin 81 mg (NSAID)

Purpose

Pain Reliever

Uses

For the temporary relief of minor aches and pains

WARNING

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use 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: Hives Facial swelling asthma (wheezing) shock

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 take a blood thinning (anticoagulant) or steroid drug take other drugs containing prescription or non prescription 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.

Do not use if you are allergic 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 gout diabetes 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 redness or swelling is present fever lasts more than 3 days new symptoms occur ringing in the ears or loss of hearing occurs

If pregnant or breast-feeding, ask a health 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:

Drink a full glass of water with each dose adults and children 12 years and over: take 1 or 2 tablets every 4 hours or 3 tablets every 6 hours, not to exceed 12 tablets in 24 hours children under 12 years: consult a doctor.

Other Information:

Store at room temperature

Inactive ingredients:

Microcrystalline Cellulose, Silicon dioxide, Talcum, Croscarmellose sodium, Stearic acid, Colloidal silicon dioxide, Titanium dioxide, Triethyl citrate, Methacrylic acid copolymer, D&C Yellow #10, FD&C Yellow #6

SPL UNCLASSIFIED SECTION

Safe pain relief

Safety enteric-coated aspirin regimen

ADULT LOW DOSE

Compare to Bayer® Aspirin active ingredient

Questions or comments?

Please call (347)378-8990 Monday Through Friday 9-5 or by Email Info@nobleotc.com

This product is not manufactured or distributed by Bayer Healthcare, LLC owner of the Registered Trademark BAYER® Tablets

TAMPER EVIDENT Do not use if safety seal under cap is broken or missing.

Manufactured for

Noble OTC LLC

Perth Amboy, NJ 08861

www.nobleotc.com

Packaging

INGREDIENTS AND APPEARANCE

NOBLEAID PAIN RELIEVER 
aspirin tablet, delayed release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81533-600
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E)	ASPIRIN	81 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER (UNII: NX76LV5T8J)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	I1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81533-600-10	100 in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2021
2	NDC: 81533-600-11	300 in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2021
3	NDC: 81533-600-30	1000 in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	11/15/2021

Labeler - Noble Otc LLC (041836435)