Proanthocyanidins (PCs), a group of polyphenolic compounds that have been studied for almost 80 years, have a high antioxidant capacity and considerable benefits to human health. These compounds are effective at scavenging free radicals in organisms and have anti-inflammatory and antiaging effects. The content of nicotinamide adenine dinucleotide (NAD+) decreases with age. Exogenous supplementation with NAD+ plays a vital role in impeding aging and prolonging lifespan; thus, NAD+ is a potential target for antiaging research. There is evidence that PCs can affect the content of NAD+, but the effects of monomeric proanthocyanidins (MPCs) and oligomeric proanthocyanidins (OPCs) on NAD+ levels are still unclear. In our study, normal human diploid skin fibroblast BJ cells were treated with MPCs and OPCs, and changes in intracellular NAD+ content were examined. Real-time qPCR was used to detect changes in the transcription of enzymes associated with NAD+ synthesis. The results showed that both MPCs and OPCs could increase NAD+ content. In low-passage BJ cells, the effects of MPCs were greater than those of OPCs. Moreover, the qPCR results showed that the mRNA expression levels of the rate-limiting enzyme NAMPT were significantly upregulated in PC-treated low-passage and senescent BJ cells, suggesting that the effect of PCs on NAD+ content may be achieved by regulating NAMPT transcription, which may provide a theoretical basis for the effect of PCs on intracellular NAD+ content.