BAYER 500 MG- aspirin powder
BAYER 500 mg by
Drug Labeling and Warnings
BAYER 500 mg by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Drug Facts
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BAYER 500 MG
aspirin powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 0280-0029 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 500 mg Inactive Ingredients Ingredient Name Strength ASPARTAME (UNII: Z0H242BBR1) ACESULFAME POTASSIUM (UNII: 23OV73Q5G9) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 0280-0029-02 2 in 1 CARTON 06/04/2015 1 1 in 1 PACKET; Type 0: Not a Combination Product 2 NDC: 0280-0029-10 10 in 1 CARTON 06/04/2015 2 1 in 1 PACKET; Type 0: Not a Combination Product 3 NDC: 0280-0029-01 100 in 1 CARTON 06/04/2015 3 1 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 06/01/2015 Labeler - Bayer HealthCare LLC (112117283)
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