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Cerelac is a brand of instant cereal made by Nestlé. The cereal is promoted for infants between 6 and 24 months old, [1] as a supplement to breast milk when it is no longer the sole item in an infant's diet. Cerelac is not a substitute for breast milk, and it is advised to continue breast feeding or infant formula along with Cerelac.
Cerelac; Cheerios [5] (in non-US/Canadian markets joint venture between General Mills and Nestlé) Chocapic [18] Cini Minis [19] Clusters [20] Cookie Crisp (in non-US ...
In 1982, Nestle began producing Cerelac in Nigeria at Agbara. Between 1984 and 1986, the company introduced baby-weaning products with higher local content, these include Cerelac Maize and Nutrend, with a mixture of soy and maize. [3] It later introduced Chocomilo, a confectionery item.
A boycott was launched in the United States on July 4, 1977, against the Swiss-based multinational food and drink processing corporation Nestlé.The boycott expanded into Europe in the early 1980s and was prompted by concerns about Nestlé's aggressive marketing of infant formulas (i.e., substitutes for breast milk), particularly in underdeveloped countries.
Gerber Products Company is an American purveyor of baby food and baby products headquartered in Fremont, Michigan. Gerber Products Company is a subsidiary of Nestlé.. Other Gerber products include breastfeeding pumps and other supplies, baby bottles and nipples, and health care products including tooth and gum cleanser and vitamin drops.
Rice cereal is the name commonly given to industrially manufactured baby food based on rice.It is also commonly used in Rice Krispy treats. Its ingredient list is not well defined and depends on the manufacturer.
This list contains a list of EC numbers for the third group, EC 3, hydrolases, placed in numerical order as determined by the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology.
The thalidomide molecule is a synthetic derivative of glutamic acid and consists of a glutarimide ring and a phthaloyl ring (Figure 5). [15] [16] Its IUPAC name is 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione and it has one chiral center [15] After thalidomide's selective inhibition of TNF-α had been reported, a renewed effort was put in thalidomide's clinical development.