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Azorubine has shown no evidence of mutagenic or carcinogenic properties and an acceptable daily intake (ADI) of 0–4 mg/kg was established in 1983 by the WHO. [10]: 19 In rare instances, it may cause skin and respiratory allergic reactions even to FDA approved dosages.
Red Only permitted for externally applied drugs and cosmetics in the US. [16] [17] [18] E126 Ponceau 6R: Red E127 Erythrosine (FD&C Red 3) Pink Approved in the EU. [8] Banned in the US. [19] E128 Red 2G: Red or pink Not approved in the EU. [11] E129 Allura Red AC (FD&C Red 40) Red Approved in the EU. [8] Banned in Switzerland. [citation needed]
CAS Number: 39366-37-5; KEGG: ... is a combined birth control pill made up of ethinylestradiol, ... This page was last edited on 30 September 2024, ...
The medication is taken by mouth and contains 30 μg EE and 3 mg DRSP per tablet (brand names Yasmin, others) or 20 μg EE and 3 mg DRSP per tablet (brand names Yaz, Yasminelle, Nikki, others). [ 2 ] [ 3 ] A formulation with levomefolic acid ( vitamin B 9 ) has also been marketed (brand names Beyaz, Safyral, others), with similar indications.
The national drug code (NDC) is a unique product identifier used in the United States for drugs intended for human use. The Drug Listing Act of 1972 [ 1 ] [ 2 ] requires registered drug establishments to provide the Food and Drug Administration (FDA) with a current list of all drugs manufactured, prepared, propagated, compounded, or processed ...
The Food and Drug Administration (FDA) has revoked the use of Red Dye No. 3 (also known as erythrosine, Red Dye 3, FD&C Red No. 3 and Red No. 3) in food and ingested drugs as of January 15 ...
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A California laboratory that analyzed confidentially submitted drug samples first detected MDMA in 1975. Over the following years the number of MDMA samples increased, eventually exceeding the number of MDA samples in the early 1980s. [257] [258] By the mid-1980s, MDMA use had spread to colleges around the United States. [251]: 33
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