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Infant Formula Act of 1980, 21 U.S.C. § 350a, is a United States statute authorizing good manufacturing practices and infant food safety for infant formula packaged and labeled in the United States. The Act of Congress amended the Federal Food, Drug, and Cosmetic Act creating section 350a under subchapter IV entitled as Food. [1]
Labels must conform with WHO/FAO guidelines on safe preparation, storage and handling of powdered infant formula (WHA resolution 61.20 [2008]). [ 8 ] In line with the recommendation for exclusive breastfeeding in WHA resolution 54.2 [2001], [ 9 ] all complementary foods must be labeled as suitable for use by infants from six months and not earlier.
If human milk is unavailable, infants should be fed iron-fortified infant formula. In addition, infants, soon after they're born, should begin receiving supplemental vitamin D. At about 6 months, infants should be introduced to nutrient-dense, complementary (and perhaps allergenic) foods. Infants and toddlers should be encouraged to consume ...
On Monday, the U.S. Food and Drug Administration (FDA) announced that, for the first time, it is setting guidelines for an acceptable level of lead in processed baby food, including canned fruit ...
A new study found that 60% of baby foods in the U.S. don't meet nutritional guidelines set by the World Health Organization (WHO). Many foods were low in protein but high in sugar and sodium.
Contraindications to breastfeeding are those conditions that could compromise the health of the infant if breast milk from their mother is consumed. Examples include galactosemia, untreated HIV, untreated active tuberculosis, Human T-lymphotropic virus 1 or II, uses illicit drugs, or mothers undergoing chemotherapy or radiation treatment.
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